Canonical Allele Identifier: CA1818251553
Gene: CCAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127210176T= , CM000670.2:g.127210176T= GRCh38
NC_000008.10:g.128222421T= , CM000670.1:g.128222421T= GRCh37
NC_000008.9:g.128291603T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_108049.1:n.460-459A=