Canonical Allele Identifier: CA13239086

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.20610679T>C , CM000672.2:g.20610679T>C	GRCh38
NC_000010.10:g.20899608T>C , CM000672.1:g.20899608T>C	GRCh37
NC_000010.9:g.20939614T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930728.1:n.1231T>C
XR_930729.1:n.1276T>C
XR_930730.1:n.1127T>C
XR_930731.1:n.1060T>C
XR_930732.1:n.1082T>C
XR_930733.1:n.1131T>C
XR_001747381.1:n.6079T>C
XR_001747382.1:n.3160T>C
XR_001747383.1:n.5422T>C
XR_001747384.2:n.5273T>C
XR_930729.2:n.2503T>C
XR_930733.2:n.5377T>C