Linked Data
dbSNP Id:
rs745749915
ExAC:
19:12761026 A / G
gnomAD v2:
19-12761026-A-G
gnomAD v3:
19-12650212-A-G
gnomAD v4:
19-12650212-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12650212A>G , CM000681.2:g.12650212A>G | GRCh38 |
| NC_000019.9:g.12761026A>G , CM000681.1:g.12761026A>G | GRCh37 |
| NC_000019.8:g.12622026A>G | NCBI36 |
| NG_008318.1:g.21566T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456935.7:c.2057T>C MANE Select | ENSP00000395473.2:p.Val686Ala | |
| ENST00000221363.8:c.2054T>C | ENSP00000221363.4:p.Val685Ala | |
| ENST00000456935.6:c.2057T>C | ENSP00000395473.2:p.Val686Ala | |
| ENST00000466794.5:n.2647T>C | ||
| NM_000528.3:c.2057T>C | NP_000519.2:p.Val686Ala | |
| NM_001173498.1:c.2054T>C | NP_001166969.1:p.Val685Ala | |
| XM_005259913.1:c.2060T>C | XP_005259970.1:p.Val687Ala | |
| XM_011528017.1:c.956T>C | XP_011526319.1:p.Val319Ala | |
| XM_005259913.2:c.2060T>C | XP_005259970.1:p.Val687Ala | |
| XM_024451518.1:c.956T>C | XP_024307286.1:p.Val319Ala | |
| NM_000528.4:c.2057T>C MANE Select | NP_000519.2:p.Val686Ala | |
| NM_001173498.2:c.2054T>C | NP_001166969.1:p.Val685Ala |