Linked Data
dbSNP Id:
rs2151216947
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73329532T>C , CM000677.2:g.73329532T>C | GRCh38 |
| NC_000015.9:g.73621873T>C , CM000677.1:g.73621873T>C | GRCh37 |
| NC_000015.8:g.71408926T>C | NCBI36 |
| NG_009063.1:g.44733A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.1590+41A>G MANE Select | ENSP00000261917.3:n.1590+41A>G | |
| ENST00000261917.3:c.1590+41A>G | ENSP00000261917.3:n.1590+41A>G | |
| NM_005477.2:c.1590+41A>G | NP_005468.1:n.1590+41A>G | |
| XM_011521148.1:c.372+41A>G | XP_011519450.1:n.372+41A>G | |
| XM_011521148.2:c.372+41A>G | XP_011519450.1:n.372+41A>G | |
| NM_005477.3:c.1590+41A>G MANE Select | NP_005468.1:n.1590+41A>G |