Canonical Allele Identifier: CA881625391

Gene:

Linked Data

• dbSNP Id: rs1434728589
• MyVariant Identifiers: chr19:g.34012889A>G (hg19) ; chr19:g.33521983A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521983A>G , CM000681.2:g.33521983A>G	GRCh38
NC_000019.9:g.34012889A>G , CM000681.1:g.34012889A>G	GRCh37
NC_000019.8:g.38704729A>G	NCBI36
NG_013358.1:g.4911T>C
NG_013358.2:g.4911T>C

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.42A>G
XR_935919.1:n.37A>G
XR_001754035.2:n.50A>G
XR_935918.2:n.50A>G