Canonical Allele Identifier: CA13772514
Gene: C12orf60 HGNC NCBI

Linked Data

dbSNP Id: rs2098435

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14851655G>A , CM000674.2:g.14851655G>A GRCh38
NC_000012.11:g.15004589G>A , CM000674.1:g.15004589G>A GRCh37
NC_000012.10:g.14895856G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000648334.1:n.125+21976G>A
ENST00000527783.1:n.76-47514G>A
ENST00000533472.1:n.86+47904G>A