Linked Data
dbSNP Id:
rs2055161541
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785771C>A , CM000681.2:g.18785771C>A | GRCh38 |
| NC_000019.9:g.18896581C>A , CM000681.1:g.18896581C>A | GRCh37 |
| NC_000019.8:g.18757581C>A | NCBI36 |
| NG_007070.1:g.10534G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1570G>T MANE Select | ENSP00000222271.2:p.Ala524Ser | |
| ENST00000222271.6:c.1570G>T | ENSP00000222271.2:p.Ala524Ser | |
| ENST00000425807.1:c.1411G>T | ENSP00000403792.1:p.Ala471Ser | |
| ENST00000542601.6:c.1471G>T | ENSP00000439156.2:p.Ala491Ser | |
| NM_000095.2:c.1570G>T | NP_000086.2:p.Ala524Ser | |
| NM_000095.3:c.1570G>T MANE Select | NP_000086.2:p.Ala524Ser |