Canonical Allele Identifier: CA1619048636
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200162C= , CM000668.2:g.31200162C= GRCh38
NC_000006.11:g.31167939C= , CM000668.1:g.31167939C= GRCh37
NC_000006.10:g.31275918C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2210C=
ENST00000414008.2:n.269C=
ENST00000424675.1:c.44+1981C=
NR_026791.1:n.124-2210C=