Canonical Allele Identifier: CA606951310

Gene:

Linked Data

• dbSNP Id: rs1255862903
• gnomAD v2: 12-93686962-G-A
• gnomAD v3: 12-93293186-G-A
• gnomAD v4: 12-93293186-G-A
• MyVariant Identifiers: chr12:g.93686962G>A (hg19) ; chr12:g.93293186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93293186G>A , CM000674.2:g.93293186G>A	GRCh38
NC_000012.11:g.93686962G>A , CM000674.1:g.93686962G>A	GRCh37
NC_000012.10:g.92211093G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040096.1:n.329+34841C>T