Canonical Allele Identifier: CA307575933

Gene:

Linked Data

• dbSNP Id: rs987635528
• MyVariant Identifiers: chr19:g.34012869G>T (hg19) ; chr19:g.33521963G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521963G>T , CM000681.2:g.33521963G>T	GRCh38
NC_000019.9:g.34012869G>T , CM000681.1:g.34012869G>T	GRCh37
NC_000019.8:g.38704709G>T	NCBI36
NG_013358.1:g.4931C>A
NG_013358.2:g.4931C>A

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.22G>T
XR_935919.1:n.17G>T
XR_001754035.2:n.30G>T
XR_935918.2:n.30G>T