Canonical Allele Identifier: CA687013164

Gene:

Linked Data

• dbSNP Id: rs1353710153
• MyVariant Identifiers: chr12:g.28198073G>T (hg19) ; chr12:g.28045140G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.28045140G>T , CM000674.2:g.28045140G>T	GRCh38
NC_000012.11:g.28198073G>T , CM000674.1:g.28198073G>T	GRCh37
NC_000012.10:g.28089340G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931460.1:n.154-6182C>A