Canonical Allele Identifier: CA1827744252
Gene:

Linked Data

dbSNP Id: rs1817919327

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787470A>G , CM000671.2:g.1787470A>G GRCh38
NC_000009.11:g.1787470A>G , CM000671.1:g.1787470A>G GRCh37
NC_000009.10:g.1777470A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68558A>G