Canonical Allele Identifier: CA783226055

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106945G>C , CM000681.2:g.1106945G>C	GRCh38
NC_000019.9:g.1106944G>C , CM000681.1:g.1106944G>C	GRCh37
NC_000019.8:g.1057944G>C	NCBI36
NG_050621.1:g.8020G>C