Canonical Allele Identifier: CA802120374

Gene:

Linked Data

• dbSNP Id: rs1405843996
• gnomAD v3: 5-113660945-T-A
• gnomAD v4: 5-113660945-T-A
• MyVariant Identifiers: chr5:g.112996642T>A (hg19) ; chr5:g.113660945T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113660945T>A , CM000667.2:g.113660945T>A	GRCh38
NC_000005.9:g.112996642T>A , CM000667.1:g.112996642T>A	GRCh37
NC_000005.8:g.113024541T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001742841.1:n.59+27581T>A