Canonical Allele Identifier: CA881625386

Gene:

Linked Data

• dbSNP Id: rs567911786
• MyVariant Identifiers: chr19:g.34012885G>A (hg19) ; chr19:g.33521979G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521979G>A , CM000681.2:g.33521979G>A	GRCh38
NC_000019.9:g.34012885G>A , CM000681.1:g.34012885G>A	GRCh37
NC_000019.8:g.38704725G>A	NCBI36
NG_013358.1:g.4915C>T
NG_013358.2:g.4915C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.38G>A
XR_935919.1:n.33G>A
XR_001754035.2:n.46G>A
XR_935918.2:n.46G>A