Canonical Allele Identifier: CA783226135

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1107052A>G , CM000681.2:g.1107052A>G	GRCh38
NC_000019.9:g.1107051A>G , CM000681.1:g.1107051A>G	GRCh37
NC_000019.8:g.1058051A>G	NCBI36
NG_050621.1:g.8127A>G