Canonical Allele Identifier: CA12151188

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96389909C>T , CM000667.2:g.96389909C>T	GRCh38
NC_000005.9:g.95725613C>T , CM000667.1:g.95725613C>T	GRCh37
NC_000005.8:g.95751369C>T	NCBI36
NG_021161.1:g.48373G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_130776.1:n.354+10257C>T