Canonical Allele Identifier: CA89976944

Gene:

Linked Data

• dbSNP Id: rs1028002490
• MyVariant Identifiers: chr3:g.187649320G>A (hg19) ; chr3:g.187931532G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931532G>A , CM000665.2:g.187931532G>A	GRCh38
NC_000003.11:g.187649320G>A , CM000665.1:g.187649320G>A	GRCh37
NC_000003.10:g.189132014G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1382C>T