Canonical Allele Identifier: CA861674128
Gene:

Linked Data

dbSNP Id: rs1331131798

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787605T>G , CM000671.2:g.1787605T>G GRCh38
NC_000009.11:g.1787605T>G , CM000671.1:g.1787605T>G GRCh37
NC_000009.10:g.1777605T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746599.1:n.142+68693T>G