Canonical Allele Identifier: CA1059430001
Gene:

Linked Data

gnomAD v3: 4-12578213-G-A
gnomAD v4: 4-12578213-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578213G>A , CM000666.2:g.12578213G>A GRCh38
NC_000004.11:g.12579837G>A , CM000666.1:g.12579837G>A GRCh37
NC_000004.10:g.12188935G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31129C>T
XR_001741374.1:n.254+44442C>T
XR_925406.3:n.140+31129C>T