Canonical Allele Identifier: CA1619048632
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200158A= , CM000668.2:g.31200158A= GRCh38
NC_000006.11:g.31167935A= , CM000668.1:g.31167935A= GRCh37
NC_000006.10:g.31275914A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2214A=
ENST00000414008.2:n.265A=
ENST00000424675.1:c.44+1977A=
NR_026791.1:n.124-2214A=