Canonical Allele Identifier: CA904086779

Gene:

Linked Data

• dbSNP Id: rs1487336709
• MyVariant Identifiers: chr3:g.187649452C>T (hg19) ; chr3:g.187931664C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931664C>T , CM000665.2:g.187931664C>T	GRCh38
NC_000003.11:g.187649452C>T , CM000665.1:g.187649452C>T	GRCh37
NC_000003.10:g.189132146C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1250G>A