Canonical Allele Identifier: CA1619048602
Gene: HCG27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200060_31200061delinsGT , CM000668.2:g.31200060_31200061delinsGT GRCh38
NC_000006.11:g.31167837_31167838delinsGT , CM000668.1:g.31167837_31167838delinsGT GRCh37
NC_000006.10:g.31275816_31275817delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2178_123+2179delinsGT
ENST00000414008.2:n.167_168delinsGT
ENST00000424675.1:c.44+1879_44+1880delinsGT
NR_026791.1:n.123+2178_123+2179delinsGT