Canonical Allele Identifier: CA786695522
Gene:

Linked Data

dbSNP Id: rs1464705620
gnomAD v3: 4-12578118-T-G
gnomAD v4: 4-12578118-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578118T>G , CM000666.2:g.12578118T>G GRCh38
NC_000004.11:g.12579742T>G , CM000666.1:g.12579742T>G GRCh37
NC_000004.10:g.12188840T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31224A>C
XR_001741374.1:n.254+44537A>C
XR_925406.3:n.140+31224A>C