Linked Data
ClinVar Variation Id:
39457
ClinVar RCV Id:
RCV000032652
dbSNP Id:
rs398122894
PubMed:
PMID:23001123
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154585323C>G , CM000663.2:g.154585323C>G | GRCh38 |
| NC_000001.10:g.154557799C>G , CM000663.1:g.154557799C>G | GRCh37 |
| NC_000001.9:g.152824423C>G | NCBI36 |
| NG_011844.1:g.47639G>C | |
| NG_011844.2:g.51238G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649042.2:c.3231G>C | ENSP00000497790.2:n.3231G>C | |
| ENST00000649724.2:c.3367G>C | ENSP00000497932.2:p.Asp1123His | |
| ENST00000680270.2:c.3220G>C | ENSP00000505532.2:p.Asp1074His | |
| ENST00000681056.2:c.2989G>C | ENSP00000506234.2:p.Asp997His | |
| ENST00000368471.8:c.2452G>C | ENSP00000357456.3:p.Asp818His | |
| ENST00000368474.9:c.3337G>C MANE Select | ENSP00000357459.4:p.Asp1113His | |
| ENST00000492630.2:n.2130G>C | ||
| ENST00000529168.2:c.3259G>C | ENSP00000431794.2:p.Asp1087His | |
| ENST00000647682.2:n.3322G>C | ||
| ENST00000648231.2:c.2452G>C | ENSP00000497555.1:p.Asp818His | |
| ENST00000648311.1:c.2452G>C | ENSP00000498137.1:p.Asp818His | |
| ENST00000648714.2:c.*812G>C | ENSP00000497434.2:n.*812G>C | |
| ENST00000649021.1:n.4073G>C | ||
| ENST00000649022.2:c.2452G>C | ENSP00000496896.2:p.Asp818His | |
| ENST00000649042.1:c.2452G>C | ENSP00000497790.1:p.Asp818His | |
| ENST00000649408.2:c.*503G>C | ENSP00000497386.2:n.*503G>C | |
| ENST00000649724.1:c.2452G>C | ENSP00000497932.1:p.Asp818His | |
| ENST00000649749.1:c.2452G>C | ENSP00000497210.1:p.Asp818His | |
| ENST00000679375.1:c.*1569G>C | ENSP00000505887.1:n.*1569G>C | |
| ENST00000679465.1:n.4198G>C | ||
| ENST00000679805.1:n.4073G>C | ||
| ENST00000679899.1:c.2395G>C | ENSP00000505996.1:p.Asp799His | |
| ENST00000680270.1:c.2452G>C | ENSP00000505532.1:p.Asp818His | |
| ENST00000680305.1:c.3154G>C | ENSP00000506312.1:p.Asp1052His | |
| ENST00000681056.1:c.2452G>C | ENSP00000506234.1:p.Asp818His | |
| ENST00000681235.1:c.*2859G>C | ENSP00000506606.1:n.*2859G>C | |
| ENST00000681429.1:n.3005G>C | ||
| ENST00000681683.1:c.2452G>C | ENSP00000506666.1:p.Asp818His | |
| ENST00000681786.1:n.4198G>C | ||
| ENST00000681901.1:c.*2937G>C | ENSP00000504883.1:n.*2937G>C | |
| ENST00000368471.7:c.2452G>C | ENSP00000357456.3:p.Asp818His | |
| ENST00000368474.8:c.3337G>C | ENSP00000357459.4:p.Asp1113His | |
| ENST00000492630.1:n.96G>C | ||
| ENST00000529168.1:c.3244G>C | ENSP00000431794.1:p.Asp1082His | |
| NM_001025107.2:c.2452G>C | NP_001020278.1:p.Asp818His | |
| NM_001111.4:c.3337G>C | NP_001102.2:p.Asp1113His | |
| NM_001193495.1:c.2452G>C | NP_001180424.1:p.Asp818His | |
| NM_015840.3:c.3259G>C | NP_056655.2:p.Asp1087His | |
| NM_015841.3:c.3202G>C | NP_056656.2:p.Asp1068His | |
| XM_006711109.1:c.3367G>C | XP_006711172.1:p.Asp1123His | |
| XM_006711111.2:c.2452G>C | XP_006711174.1:p.Asp818His | |
| XM_006711112.1:c.2452G>C | XP_006711175.1:p.Asp818His | |
| XM_006711113.1:c.2452G>C | XP_006711176.1:p.Asp818His | |
| XM_011509060.1:c.3466G>C | XP_011507362.1:p.Asp1156His | |
| XM_011509061.1:c.3388G>C | XP_011507363.1:p.Asp1130His | |
| XM_011509062.1:c.3355G>C | XP_011507364.1:p.Asp1119His | |
| NM_001025107.3:c.2452G>C | NP_001020278.1:p.Asp818His | |
| NM_001111.5:c.3337G>C MANE Select | NP_001102.3:p.Asp1113His | |
| NM_001193495.2:c.2452G>C | NP_001180424.1:p.Asp818His | |
| NM_001365045.1:c.3364G>C | NP_001351974.1:p.Asp1122His | |
| NM_001365046.1:c.2452G>C | NP_001351975.1:p.Asp818His | |
| NM_001365047.1:c.2452G>C | NP_001351976.1:p.Asp818His | |
| NM_001365048.1:c.2452G>C | NP_001351977.1:p.Asp818His | |
| NM_001365049.1:c.2374G>C | NP_001351978.1:p.Asp792His | |
| NM_015840.4:c.3259G>C | NP_056655.3:p.Asp1087His | |
| NM_015841.4:c.3202G>C | NP_056656.3:p.Asp1068His | |
| XM_006711113.2:c.2452G>C | XP_006711176.1:p.Asp818His | |
| XM_011509061.2:c.2374G>C | XP_011507363.2:p.Asp792His | |
| XM_024449674.1:c.3466G>C | XP_024305442.1:p.Asp1156His |