Canonical Allele Identifier: CA536097431

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136218685T>G , CM000664.2:g.136218685T>G	GRCh38
NC_000002.11:g.136976255T>G , CM000664.1:g.136976255T>G	GRCh37
NC_000002.10:g.136692725T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739716.1:n.901+3549T>G