Canonical Allele Identifier: CA16956841

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2567423G>T , CM000663.2:g.2567423G>T	GRCh38
NC_000001.10:g.2498862G>T , CM000663.1:g.2498862G>T	GRCh37
NC_000001.9:g.2475556C>A	NCBI36
NG_047096.1:g.16059G>T

Transcript Alleles

HGVS	Amino-acid Change
NR_121638.1:n.71+818G>T