Canonical Allele Identifier: CA1619048580
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31199979C= , CM000668.2:g.31199979C= GRCh38
NC_000006.11:g.31167756C= , CM000668.1:g.31167756C= GRCh37
NC_000006.10:g.31275735C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2097C=
ENST00000414008.2:n.86C=
ENST00000424675.1:c.44+1798C=
NR_026791.1:n.123+2097C=