Canonical Allele Identifier: CA1827744245
Gene:

Linked Data

dbSNP Id: rs1586626157

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787465C>G , CM000671.2:g.1787465C>G GRCh38
NC_000009.11:g.1787465C>G , CM000671.1:g.1787465C>G GRCh37
NC_000009.10:g.1777465C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68553C>G