Canonical Allele Identifier: CA693572552

Gene:

Linked Data

• dbSNP Id: rs1375005023
• MyVariant Identifiers: chr12:g.93686985C>A (hg19) ; chr12:g.93293209C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93293209C>A , CM000674.2:g.93293209C>A	GRCh38
NC_000012.11:g.93686985C>A , CM000674.1:g.93686985C>A	GRCh37
NC_000012.10:g.92211116C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040096.1:n.329+34818G>T