Canonical Allele Identifier: CA307575959

Gene:

Linked Data

• dbSNP Id: rs1045400420
• MyVariant Identifiers: chr19:g.34012888C>T (hg19) ; chr19:g.33521982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521982C>T , CM000681.2:g.33521982C>T	GRCh38
NC_000019.9:g.34012888C>T , CM000681.1:g.34012888C>T	GRCh37
NC_000019.8:g.38704728C>T	NCBI36
NG_013358.1:g.4912G>A
NG_013358.2:g.4912G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.41C>T
XR_935919.1:n.36C>T
XR_001754035.2:n.49C>T
XR_935918.2:n.49C>T