Canonical Allele Identifier: CA1059430064
Gene:

Linked Data

dbSNP Id: rs1577128574
gnomAD v3: 4-12578350-G-A
gnomAD v4: 4-12578350-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578350G>A , CM000666.2:g.12578350G>A GRCh38
NC_000004.11:g.12579974G>A , CM000666.1:g.12579974G>A GRCh37
NC_000004.10:g.12189072G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+30992C>T
XR_001741374.1:n.254+44305C>T
XR_925406.3:n.140+30992C>T