Linked Data
ClinVar Variation Id:
566223
dbSNP Id:
rs745777805
ExAC:
18:21125028 G / A
gnomAD v2:
18-21125028-G-A
gnomAD v4:
18-23545064-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23545064G>A , CM000680.2:g.23545064G>A | GRCh38 |
| NC_000018.9:g.21125028G>A , CM000680.1:g.21125028G>A | GRCh37 |
| NC_000018.8:g.19379026G>A | NCBI36 |
| NG_012795.1:g.46554C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269228.10:c.1843C>T MANE Select | ENSP00000269228.4:p.Arg615Cys | |
| ENST00000269228.9:c.1843C>T | ENSP00000269228.4:p.Arg615Cys | |
| ENST00000540608.5:n.1757C>T | ||
| ENST00000591051.1:c.921C>T | ||
| NM_000271.4:c.1843C>T | NP_000262.2:p.Arg615Cys | |
| XM_005258277.1:c.1894C>T | XP_005258334.1:p.Arg632Cys | |
| XM_005258278.3:c.1894C>T | XP_005258335.1:p.Arg632Cys | |
| XM_005258279.1:c.1843C>T | XP_005258336.1:p.Arg615Cys | |
| XM_006722479.2:c.1894C>T | XP_006722542.1:p.Arg632Cys | |
| XM_011526015.1:c.1429C>T | XP_011524317.1:p.Arg477Cys | |
| XM_005258278.5:c.1894C>T | XP_005258335.1:p.Arg632Cys | |
| XM_005258279.2:c.1843C>T | XP_005258336.1:p.Arg615Cys | |
| XM_006722479.3:c.1894C>T | XP_006722542.1:p.Arg632Cys | |
| XM_017025784.1:c.1894C>T | XP_016881273.1:p.Arg632Cys | |
| XM_017025785.1:c.1894C>T | XP_016881274.1:p.Arg632Cys | |
| XM_017025786.1:c.1843C>T | XP_016881275.1:p.Arg615Cys | |
| XM_017025787.1:c.1843C>T | XP_016881276.1:p.Arg615Cys | |
| NM_000271.5:c.1843C>T MANE Select | NP_000262.2:p.Arg615Cys |