Canonical Allele Identifier: CA714628900

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61578744C>G , CM000677.2:g.61578744C>G	GRCh38
NC_000015.9:g.61870943C>G , CM000677.1:g.61870943C>G	GRCh37
NC_000015.8:g.59658235C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751569.1:n.240+11172G>C
XR_001751570.1:n.438+11172G>C