Canonical Allele Identifier: CA1880834429
Gene:

Linked Data

dbSNP Id: rs1483145908

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576881C>G , CM000671.2:g.129576881C>G GRCh38
NC_000009.11:g.132339160C>G , CM000671.1:g.132339160C>G GRCh37
NC_000009.10:g.131378981C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1283C>G