Linked Data
dbSNP Id:
rs1311011150
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125325A>C , CM000666.2:g.55125325A>C | GRCh38 |
| NC_000004.11:g.55991492A>C , CM000666.1:g.55991492A>C | GRCh37 |
| NC_000004.10:g.55686249A>C | NCBI36 |
| NG_012004.1:g.5271T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-32T>G MANE Select | ENSP00000263923.4:n.-32T>G | |
| ENST00000263923.4:c.-32T>G | ENSP00000263923.4:n.-32T>G | |
| NM_002253.2:c.-32T>G | NP_002244.1:n.-32T>G | |
| NM_002253.3:c.-32T>G | NP_002244.1:n.-32T>G | |
| NM_002253.4:c.-32T>G MANE Select | NP_002244.1:n.-32T>G |