Canonical Allele Identifier: CA2735687939

Gene:

Linked Data

• dbSNP Id: rs2122720720

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218360A>G , CM000681.2:g.20218360A>G	GRCh38
NC_000019.9:g.20329169A>G , CM000681.1:g.20329169A>G	GRCh37
NC_000019.8:g.20190169A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-1044T>C
XR_936389.1:n.502-1044T>C
XR_936390.1:n.511-1044T>C
XR_936391.1:n.514-1044T>C
XR_936392.1:n.514-1044T>C
XR_936394.1:n.41-374A>G
XR_001754063.2:n.1506-1044T>C
XR_001754064.2:n.138-1044T>C
XR_001754066.1:n.3912-1044T>C
XR_001754067.1:n.3912-1044T>C
XR_001754068.1:n.3912-1044T>C
XR_936394.2:n.41-374A>G
XR_936406.2:n.1411-1044T>C