Canonical Allele Identifier: CA785787033

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.11628425T>G , CM000666.2:g.11628425T>G	GRCh38
NC_000004.11:g.11630049T>G , CM000666.1:g.11630049T>G	GRCh37
NC_000004.10:g.11239147T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741361.1:n.1026+76471T>G