Canonical Allele Identifier: CA714620951

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61708933A>T , CM000677.2:g.61708933A>T	GRCh38
NC_000015.9:g.62001132A>T , CM000677.1:g.62001132A>T	GRCh37
NC_000015.8:g.59788424A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751569.1:n.77+6182T>A