Canonical Allele Identifier: CA1619157089
Gene:

Linked Data

dbSNP Id: rs1761781330

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439831G>A , CM000668.2:g.31439831G>A GRCh38
NC_000006.11:g.31407608G>A , CM000668.1:g.31407608G>A GRCh37
NC_000006.10:g.31515587G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.276C>T