Canonical Allele Identifier: CA13892175

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110817691G>A , CM000675.2:g.110817691G>A	GRCh38
NC_000013.10:g.111470038G>A , CM000675.1:g.111470038G>A	GRCh37
NC_000013.9:g.110268039G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011521138.1:c.941-1099G>A	XP_011519440.1:n.941-1099G>A
XM_011521139.1:c.794-1099G>A	XP_011519441.1:n.794-1099G>A
XM_011521140.1:c.707-1099G>A	XP_011519442.1:n.707-1099G>A
XM_011521141.1:c.513-1099G>A	XP_011519443.1:n.513-1099G>A
XR_931727.1:n.1793-1099G>A
XR_931728.1:n.1400-1099G>A
NR_158538.1:n.70-1099G>A
XR_001750021.1:n.4393G>A