Canonical Allele Identifier: CA881625590

Gene:

Linked Data

• dbSNP Id: rs1357173161
• MyVariant Identifiers: chr19:g.34012992T>A (hg19) ; chr19:g.33522086T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33522086T>A , CM000681.2:g.33522086T>A	GRCh38
NC_000019.9:g.34012992T>A , CM000681.1:g.34012992T>A	GRCh37
NC_000019.8:g.38704832T>A	NCBI36
NG_013358.1:g.4808A>T
NG_013358.2:g.4808A>T

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.73+72T>A
XR_935919.1:n.72+68T>A
XR_001754035.2:n.81+72T>A
XR_935918.2:n.81+72T>A