Canonical Allele Identifier: CA549812901
Gene:

Linked Data

dbSNP Id: rs1303793783
gnomAD v2: 4-12579811-C-A
gnomAD v3: 4-12578187-C-A
gnomAD v4: 4-12578187-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578187C>A , CM000666.2:g.12578187C>A GRCh38
NC_000004.11:g.12579811C>A , CM000666.1:g.12579811C>A GRCh37
NC_000004.10:g.12188909C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31155G>T
XR_001741374.1:n.254+44468G>T
XR_925406.3:n.140+31155G>T