Linked Data
dbSNP Id:
rs897757195
gnomAD v2:
16-4812283-C-A
gnomAD v3:
16-4762282-C-A
gnomAD v4:
16-4762282-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.4762282C>A , CM000678.2:g.4762282C>A | GRCh38 |
| NC_000016.9:g.4812283C>A , CM000678.1:g.4812283C>A | GRCh37 |
| NC_000016.8:g.4752284C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219478.11:c.652G>T MANE Select | ENSP00000219478.5:p.Ala218Ser | |
| ENST00000219478.10:c.652G>T | ENSP00000219478.5:p.Ala218Ser | |
| ENST00000545009.1:c.652G>T | ENSP00000445714.1:p.Ala218Ser | |
| ENST00000589422.1:c.*180G>T | ENSP00000466375.1:n.*180G>T | |
| NM_001303450.1:c.652G>T | NP_001290379.1:p.Ala218Ser | |
| NM_021646.2:c.652G>T | NP_067678.1:p.Ala218Ser | |
| XM_005255243.2:c.301G>T | XP_005255300.1:p.Ala101Ser | |
| XM_011522453.1:c.652G>T | XP_011520755.1:p.Ala218Ser | |
| XM_011522454.1:c.28G>T | XP_011520756.1:p.Ala10Ser | |
| NM_021646.3:c.652G>T | NP_067678.1:p.Ala218Ser | |
| XM_005255243.4:c.301G>T | XP_005255300.1:p.Ala101Ser | |
| XM_011522453.2:c.652G>T | XP_011520755.1:p.Ala218Ser | |
| XM_011522454.3:c.28G>T | XP_011520756.1:p.Ala10Ser | |
| XM_017023121.2:c.28G>T | XP_016878610.1:p.Ala10Ser | |
| NM_001303450.2:c.652G>T | NP_001290379.1:p.Ala218Ser | |
| NM_021646.4:c.652G>T MANE Select | NP_067678.1:p.Ala218Ser |