Linked Data
dbSNP Id:
rs60369023
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.20604981G>T , CM000663.2:g.20604981G>T | GRCh38 |
| NC_000001.10:g.20931474G>T , CM000663.1:g.20931474G>T | GRCh37 |
| NC_000001.9:g.20804061G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375071.4:c.208G>T MANE Select | ENSP00000364212.3:p.Ala70Ser | |
| ENST00000375071.3:c.208G>T | ENSP00000364212.3:p.Ala70Ser | |
| ENST00000461985.1:n.252G>T | ||
| NM_001785.2:c.208G>T | NP_001776.1:p.Ala70Ser | |
| NM_001785.3:c.208G>T MANE Select | NP_001776.1:p.Ala70Ser |