Canonical Allele Identifier: CA824061155

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33518955G>C , CM000668.2:g.33518955G>C	GRCh38
NC_000006.11:g.33486732G>C , CM000668.1:g.33486732G>C	GRCh37
NC_000006.10:g.33594710G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743876.1:n.144+410C>G