Canonical Allele Identifier: CA2770501478
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200056T>G , CM000668.2:g.31200056T>G GRCh38
NC_000006.11:g.31167833T>G , CM000668.1:g.31167833T>G GRCh37
NC_000006.10:g.31275812T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2174T>G
ENST00000414008.2:n.163T>G
ENST00000424675.1:c.44+1875T>G
NR_026791.1:n.123+2174T>G