Linked Data
ClinVar Variation Id:
466249
dbSNP Id:
rs148641800
ExAC:
18:43492273 C / T
gnomAD v2:
18-43492273-C-T
gnomAD v3:
18-45912308-C-T
gnomAD v4:
18-45912308-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.45912308C>T , CM000680.2:g.45912308C>T | GRCh38 |
| NC_000018.9:g.43492273C>T , CM000680.1:g.43492273C>T | GRCh37 |
| NC_000018.8:g.41746271C>T | NCBI36 |
| NG_042838.1:g.60032G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000586655.2:n.2149G>A | ||
| ENST00000587884.2:c.3965G>A | ENSP00000466990.2:p.Arg1322His | |
| ENST00000590884.6:c.3965G>A | ENSP00000466403.2:p.Arg1322His | |
| ENST00000592272.6:c.3965G>A | ENSP00000467464.2:p.Arg1322His | |
| ENST00000696482.1:c.3705G>A | ENSP00000512656.1:n.3705G>A | |
| ENST00000696483.1:c.3965G>A | ENSP00000512657.1:p.Arg1322His | |
| ENST00000696484.1:c.3965G>A | ENSP00000512658.1:p.Arg1322His | |
| ENST00000696485.1:c.3965G>A | ENSP00000512659.1:p.Arg1322His | |
| ENST00000696489.1:c.3965G>A | ENSP00000512660.1:p.Arg1322His | |
| ENST00000696490.1:c.3965G>A | ENSP00000512661.1:p.Arg1322His | |
| ENST00000282041.11:c.3965G>A MANE Select | ENSP00000282041.4:p.Arg1322His | |
| ENST00000282041.9:c.3965G>A | ENSP00000282041.4:p.Arg1322His | |
| ENST00000585906.5:n.744G>A | ||
| ENST00000587884.1:c.590G>A | ENSP00000466990.1:p.Arg197His | |
| ENST00000587974.1:n.4000G>A | ||
| ENST00000590884.5:c.590G>A | ENSP00000466403.1:p.Arg197His | |
| ENST00000592272.5:c.590G>A | ENSP00000467464.1:p.Arg197His | |
| NM_020964.2:c.3965G>A | NP_066015.2:p.Arg1322His | |
| XM_011526120.1:c.3965G>A | XP_011524422.1:p.Arg1322His | |
| XM_011526121.1:c.3965G>A | XP_011524423.1:p.Arg1322His | |
| XM_011526122.1:c.3965G>A | XP_011524424.1:p.Arg1322His | |
| XM_011526123.1:c.3965G>A | XP_011524425.1:p.Arg1322His | |
| XM_011526124.1:c.3965G>A | XP_011524426.1:p.Arg1322His | |
| XM_011526125.1:c.3824G>A | XP_011524427.1:p.Arg1275His | |
| XM_011526126.1:c.2900G>A | XP_011524428.1:p.Arg967His | |
| XM_011526127.1:c.3965G>A | XP_011524429.1:p.Arg1322His | |
| XM_011526128.1:c.3965G>A | XP_011524430.1:p.Arg1322His | |
| XR_935244.1:n.4065G>A | ||
| NM_020964.3:c.3965G>A MANE Select | NP_066015.2:p.Arg1322His | |
| XM_017025889.1:c.3965G>A | XP_016881378.1:p.Arg1322His | |
| XM_017025890.2:c.3965G>A | XP_016881379.1:p.Arg1322His | |
| XM_017025891.1:c.3824G>A | XP_016881380.1:p.Arg1275His | |
| XM_017025892.1:c.2900G>A | XP_016881381.1:p.Arg967His | |
| XM_017025893.1:c.590G>A | XP_016881382.1:p.Arg197His | |
| XR_001753256.1:n.4047G>A | ||
| XR_001753257.1:n.4047G>A |