Canonical Allele Identifier: CA424211844

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.247184887C>G , CM000663.2:g.247184887C>G	GRCh38
NC_000001.10:g.247348189C>G , CM000663.1:g.247348189C>G	GRCh37
NC_000001.9:g.245414812C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400933.2:n.596G>C