Linked Data
ClinVar Variation Id:
1980107
ClinVar RCV Id:
RCV002756387
dbSNP Id:
rs200710797
ExAC:
18:7015736 C / T
gnomAD v2:
18-7015736-C-T
gnomAD v3:
18-7015737-C-T
gnomAD v4:
18-7015737-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.7015737C>T , CM000680.2:g.7015737C>T | GRCh38 |
| NC_000018.9:g.7015736C>T , CM000680.1:g.7015736C>T | GRCh37 |
| NC_000018.8:g.7005736C>T | NCBI36 |
| NG_034251.1:g.107078G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389658.4:c.3111G>A MANE Select | ENSP00000374309.3:p.Ala1037= | |
| ENST00000389658.3:c.3111G>A | ENSP00000374309.3:p.Ala1037= | |
| ENST00000579014.5:n.4126G>A | ||
| NM_005559.3:c.3111G>A | NP_005550.2:p.Ala1037= | |
| XM_011525655.1:c.3111G>A | XP_011523957.1:p.Ala1037= | |
| XM_011525656.1:c.1539G>A | XP_011523958.1:p.Ala513= | |
| XM_011525657.1:c.3111G>A | XP_011523959.1:p.Ala1037= | |
| XM_011525655.2:c.3111G>A | XP_011523957.1:p.Ala1037= | |
| XM_011525656.2:c.1539G>A | XP_011523958.1:p.Ala513= | |
| NM_005559.4:c.3111G>A MANE Select | NP_005550.2:p.Ala1037= |