Canonical Allele Identifier: CA603939647

Gene:

Linked Data

• dbSNP Id: rs1179377743
• gnomAD v2: 12-24770847-T-A
• gnomAD v3: 12-24617913-T-A
• gnomAD v4: 12-24617913-T-A
• MyVariant Identifiers: chr12:g.24770847T>A (hg19) ; chr12:g.24617913T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.24617913T>A , CM000674.2:g.24617913T>A	GRCh38
NC_000012.11:g.24770847T>A , CM000674.1:g.24770847T>A	GRCh37
NC_000012.10:g.24662114T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001749046.1:n.425-103A>T