Canonical Allele Identifier: CA1096188128

Gene:

Linked Data

• dbSNP Id: rs1778857800
• gnomAD v3: 6-155812567-C-A
• gnomAD v4: 6-155812567-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812567C>A , CM000668.2:g.155812567C>A	GRCh38
NC_000006.11:g.156133701C>A , CM000668.1:g.156133701C>A	GRCh37
NC_000006.10:g.156175393C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19148C>A
XR_943146.1:n.645-528G>T
XR_001744423.1:n.699-528G>T
XR_001744424.1:n.79+19148C>A