Canonical Allele Identifier: CA1827744204
Gene:

Linked Data

dbSNP Id: rs1352723671

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787413G>A , CM000671.2:g.1787413G>A GRCh38
NC_000009.11:g.1787413G>A , CM000671.1:g.1787413G>A GRCh37
NC_000009.10:g.1777413G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68501G>A