Canonical Allele Identifier: CA783226125

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1107040G>C , CM000681.2:g.1107040G>C	GRCh38
NC_000019.9:g.1107039G>C , CM000681.1:g.1107039G>C	GRCh37
NC_000019.8:g.1058039G>C	NCBI36
NG_050621.1:g.8115G>C