Canonical Allele Identifier: CA76316049

Gene:

Linked Data

• dbSNP Id: rs911771199
• MyVariant Identifiers: chr3:g.61413740A>G (hg19) ; chr3:g.61428066A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.61428066A>G , CM000665.2:g.61428066A>G	GRCh38
NC_000003.11:g.61413740A>G , CM000665.1:g.61413740A>G	GRCh37
NC_000003.10:g.61388780A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_940892.1:n.165-380T>C
XR_940893.1:n.164+448T>C
XR_001740725.1:n.202+448T>C
XR_940892.2:n.203-380T>C