Linked Data
dbSNP Id:
rs1227423324
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.175441445C>G , CM000667.2:g.175441445C>G | GRCh38 |
| NC_000005.9:g.174868448C>G , CM000667.1:g.174868448C>G | GRCh37 |
| NC_000005.8:g.174801054C>G | NCBI36 |
| NG_011802.1:g.7716G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393752.3:c.*314G>C MANE Select | ENSP00000377353.1:n.*314G>C | |
| ENST00000393752.2:c.*314G>C | ENSP00000377353.1:n.*314G>C | |
| NM_000794.3:c.*314G>C | NP_000785.1:n.*314G>C | |
| NM_000794.4:c.*314G>C | NP_000785.1:n.*314G>C | |
| NM_000794.5:c.*314G>C MANE Select | NP_000785.1:n.*314G>C |