Canonical Allele Identifier: CA127628866

Gene:

Linked Data

• dbSNP Id: rs998835547
• gnomAD v2: 5-128722730-G-A
• gnomAD v3: 5-129387037-G-A
• gnomAD v4: 5-129387037-G-A
• MyVariant Identifiers: chr5:g.128722730G>A (hg19) ; chr5:g.129387037G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.129387037G>A , CM000667.2:g.129387037G>A	GRCh38
NC_000005.9:g.128722730G>A , CM000667.1:g.128722730G>A	GRCh37
NC_000005.8:g.128750629G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427770.2:n.163-1411G>A
XR_948774.1:n.235-5614G>A
XR_001742463.1:n.4089-1411G>A
XR_001742464.1:n.2019-5614G>A
XR_001742465.1:n.401-1411G>A
XR_427770.3:n.337-1411G>A