Canonical Allele Identifier: CA1880834516
Gene:

Linked Data

dbSNP Id: rs1829780046

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576941C>G , CM000671.2:g.129576941C>G GRCh38
NC_000009.11:g.132339220C>G , CM000671.1:g.132339220C>G GRCh37
NC_000009.10:g.131379041C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1343C>G