Canonical Allele Identifier: CA274826996

Gene: C15orf32

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92501109T>C , CM000677.2:g.92501109T>C	GRCh38
NC_000015.9:g.93044339T>C , CM000677.1:g.93044339T>C	GRCh37
NC_000015.8:g.90845343T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001301106.1:c.*786T>C	NP_001288035.1:n.*786T>C
NM_153040.2:c.*709T>C	NP_694585.1:n.*709T>C
NR_161370.1:n.1718T>C
NR_161371.1:n.1756T>C