Linked Data
dbSNP Id:
rs1572217604
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652674T>G , CM000663.2:g.171652674T>G | GRCh38 |
| NC_000001.10:g.171621814T>G , CM000663.1:g.171621814T>G | GRCh37 |
| NC_000001.9:g.169888437T>G | NCBI36 |
| NG_008859.1:g.4960A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.-63A>C MANE Select | ENSP00000037502.5:n.-63A>C | |
| ENST00000037502.10:c.-63A>C | ENSP00000037502.5:n.-63A>C | |
| NM_000261.2:c.-63A>C MANE Select | NP_000252.1:n.-63A>C |