Canonical Allele Identifier: CA1059429912
Gene:

Linked Data

dbSNP Id: rs1711580236
gnomAD v3: 4-12578028-G-A
gnomAD v4: 4-12578028-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578028G>A , CM000666.2:g.12578028G>A GRCh38
NC_000004.11:g.12579652G>A , CM000666.1:g.12579652G>A GRCh37
NC_000004.10:g.12188750G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31314C>T
XR_001741374.1:n.254+44627C>T
XR_925406.3:n.140+31314C>T