Canonical Allele Identifier: CA1827744343
Gene:

Linked Data

dbSNP Id: rs1281632976

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787612T>A , CM000671.2:g.1787612T>A GRCh38
NC_000009.11:g.1787612T>A , CM000671.1:g.1787612T>A GRCh37
NC_000009.10:g.1777612T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746599.1:n.142+68700T>A