Canonical Allele Identifier: CA682822711

Gene:

Linked Data

• dbSNP Id: rs946574351
• gnomAD v3: 12-102501568-G-T
• gnomAD v4: 12-102501568-G-T
• MyVariant Identifiers: chr12:g.102895346G>T (hg19) ; chr12:g.102501568G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102501568G>T , CM000674.2:g.102501568G>T	GRCh38
NC_000012.11:g.102895346G>T , CM000674.1:g.102895346G>T	GRCh37
NC_000012.10:g.101419476G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001749289.1:n.1952+17680G>T