MyVariant.info:
GRCh37
chr1:g.154557477A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154585001A>G , CM000663.2:g.154585001A>G | GRCh38 |
| NC_000001.10:g.154557477A>G , CM000663.1:g.154557477A>G | GRCh37 |
| NC_000001.9:g.152824101A>G | NCBI36 |
| NG_011844.1:g.47961T>C | |
| NG_011844.2:g.51560T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649042.2:c.3380T>C | ENSP00000497790.2:n.3380T>C | |
| ENST00000649724.2:c.3516T>C | ENSP00000497932.2:p.Phe1172= | |
| ENST00000680270.2:c.3369T>C | ENSP00000505532.2:p.Phe1123= | |
| ENST00000681056.2:c.3138T>C | ENSP00000506234.2:p.Phe1046= | |
| ENST00000368471.8:c.2601T>C | ENSP00000357456.3:p.Phe867= | |
| ENST00000368474.9:c.3486T>C MANE Select | ENSP00000357459.4:p.Phe1162= | |
| ENST00000492630.2:n.2279T>C | ||
| ENST00000529168.2:c.3408T>C | ENSP00000431794.2:p.Phe1136= | |
| ENST00000647682.2:n.3471T>C | ||
| ENST00000648231.2:c.2601T>C | ENSP00000497555.1:p.Phe867= | |
| ENST00000648311.1:c.2601T>C | ENSP00000498137.1:p.Phe867= | |
| ENST00000648714.2:c.*961T>C | ENSP00000497434.2:n.*961T>C | |
| ENST00000649021.1:n.4222T>C | ||
| ENST00000649022.2:c.2601T>C | ENSP00000496896.2:p.Phe867= | |
| ENST00000649042.1:c.2601T>C | ENSP00000497790.1:p.Phe867= | |
| ENST00000649408.2:c.*652T>C | ENSP00000497386.2:n.*652T>C | |
| ENST00000649724.1:c.2601T>C | ENSP00000497932.1:p.Phe867= | |
| ENST00000649749.1:c.2601T>C | ENSP00000497210.1:p.Phe867= | |
| ENST00000679375.1:c.*1718T>C | ENSP00000505887.1:n.*1718T>C | |
| ENST00000679465.1:n.4347T>C | ||
| ENST00000679805.1:n.4222T>C | ||
| ENST00000679899.1:c.2544T>C | ENSP00000505996.1:p.Phe848= | |
| ENST00000680270.1:c.2601T>C | ENSP00000505532.1:p.Phe867= | |
| ENST00000680305.1:c.3303T>C | ENSP00000506312.1:p.Phe1101= | |
| ENST00000681056.1:c.2601T>C | ENSP00000506234.1:p.Phe867= | |
| ENST00000681235.1:c.*3008T>C | ENSP00000506606.1:n.*3008T>C | |
| ENST00000681429.1:n.3154T>C | ||
| ENST00000681683.1:c.2601T>C | ENSP00000506666.1:p.Phe867= | |
| ENST00000681786.1:n.4347T>C | ||
| ENST00000681901.1:c.*3086T>C | ENSP00000504883.1:n.*3086T>C | |
| ENST00000368471.7:c.2601T>C | ENSP00000357456.3:p.Phe867= | |
| ENST00000368474.8:c.3486T>C | ENSP00000357459.4:p.Phe1162= | |
| ENST00000492630.1:n.245T>C | ||
| ENST00000529168.1:c.3393T>C | ENSP00000431794.1:p.Phe1131= | |
| NM_001025107.2:c.2601T>C | NP_001020278.1:p.Phe867= | |
| NM_001111.4:c.3486T>C | NP_001102.2:p.Phe1162= | |
| NM_001193495.1:c.2601T>C | NP_001180424.1:p.Phe867= | |
| NM_015840.3:c.3408T>C | NP_056655.2:p.Phe1136= | |
| NM_015841.3:c.3351T>C | NP_056656.2:p.Phe1117= | |
| XM_006711109.1:c.3516T>C | XP_006711172.1:p.Phe1172= | |
| XM_006711111.2:c.2601T>C | XP_006711174.1:p.Phe867= | |
| XM_006711112.1:c.2601T>C | XP_006711175.1:p.Phe867= | |
| XM_006711113.1:c.2601T>C | XP_006711176.1:p.Phe867= | |
| XM_011509060.1:c.3615T>C | XP_011507362.1:p.Phe1205= | |
| XM_011509061.1:c.3537T>C | XP_011507363.1:p.Phe1179= | |
| XM_011509062.1:c.3504T>C | XP_011507364.1:p.Phe1168= | |
| NM_001025107.3:c.2601T>C | NP_001020278.1:p.Phe867= | |
| NM_001111.5:c.3486T>C MANE Select | NP_001102.3:p.Phe1162= | |
| NM_001193495.2:c.2601T>C | NP_001180424.1:p.Phe867= | |
| NM_001365045.1:c.3513T>C | NP_001351974.1:p.Phe1171= | |
| NM_001365046.1:c.2601T>C | NP_001351975.1:p.Phe867= | |
| NM_001365047.1:c.2601T>C | NP_001351976.1:p.Phe867= | |
| NM_001365048.1:c.2601T>C | NP_001351977.1:p.Phe867= | |
| NM_001365049.1:c.2523T>C | NP_001351978.1:p.Phe841= | |
| NM_015840.4:c.3408T>C | NP_056655.3:p.Phe1136= | |
| NM_015841.4:c.3351T>C | NP_056656.3:p.Phe1117= | |
| XM_006711113.2:c.2601T>C | XP_006711176.1:p.Phe867= | |
| XM_011509061.2:c.2523T>C | XP_011507363.2:p.Phe841= | |
| XM_024449674.1:c.3615T>C | XP_024305442.1:p.Phe1205= |