Canonical Allele Identifier: CA307575946

Gene:

Linked Data

• dbSNP Id: rs915284539
• MyVariant Identifiers: chr19:g.34012882C>T (hg19) ; chr19:g.33521976C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521976C>T , CM000681.2:g.33521976C>T	GRCh38
NC_000019.9:g.34012882C>T , CM000681.1:g.34012882C>T	GRCh37
NC_000019.8:g.38704722C>T	NCBI36
NG_013358.1:g.4918G>A
NG_013358.2:g.4918G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.35C>T
XR_935919.1:n.30C>T
XR_001754035.2:n.43C>T
XR_935918.2:n.43C>T