Canonical Allele Identifier: CA309668901

Gene:

Linked Data

• dbSNP Id: rs925104450
• MyVariant Identifiers: chr19:g.51340640G>A (hg19) ; chr19:g.50837384G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50837384G>A , CM000681.2:g.50837384G>A	GRCh38
NC_000019.9:g.51340640G>A , CM000681.1:g.51340640G>A	GRCh37
NC_000019.8:g.56032452G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_131203.1:n.213+6091G>A
NR_131205.1:n.230+6091G>A
XR_936030.1:n.298+6091G>A
XR_936031.1:n.298+6091G>A
XR_936032.1:n.298+6091G>A
XR_936033.1:n.294+6091G>A
XR_936035.1:n.281+6091G>A