Canonical Allele Identifier: CA1619048612
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200087T= , CM000668.2:g.31200087T= GRCh38
NC_000006.11:g.31167864T= , CM000668.1:g.31167864T= GRCh37
NC_000006.10:g.31275843T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2205T=
ENST00000414008.2:n.194T=
ENST00000424675.1:c.44+1906T=
NR_026791.1:n.123+2205T=