Canonical Allele Identifier: CA909017109

Gene:

Linked Data

• dbSNP Id: rs1295064428
• gnomAD v3: 3-61428088-A-G
• gnomAD v4: 3-61428088-A-G
• MyVariant Identifiers: chr3:g.61413762A>G (hg19) ; chr3:g.61428088A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.61428088A>G , CM000665.2:g.61428088A>G	GRCh38
NC_000003.11:g.61413762A>G , CM000665.1:g.61413762A>G	GRCh37
NC_000003.10:g.61388802A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_940892.1:n.165-402T>C
XR_940893.1:n.164+426T>C
XR_001740725.1:n.202+426T>C
XR_940892.2:n.203-402T>C