Canonical Allele Identifier: CA880474312

Gene:

Linked Data

• dbSNP Id: rs1428331933
• MyVariant Identifiers: chr19:g.20218122A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218122A>T , CM000681.2:g.20218122A>T	GRCh38
NC_000019.9:g.20328931A>T , CM000681.1:g.20328931A>T	GRCh37
NC_000019.8:g.20189931A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-806T>A
XR_936389.1:n.502-806T>A
XR_936390.1:n.511-806T>A
XR_936391.1:n.514-806T>A
XR_936392.1:n.514-806T>A
XR_936394.1:n.41-612A>T
XR_001754063.2:n.1506-806T>A
XR_001754064.2:n.138-806T>A
XR_001754066.1:n.3912-806T>A
XR_001754067.1:n.3912-806T>A
XR_001754068.1:n.3912-806T>A
XR_936394.2:n.41-612A>T
XR_936406.2:n.1411-806T>A