Canonical Allele Identifier: CA1087424246
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1779820103

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200062del , CM000668.2:g.31200062del GRCh38
NC_000006.11:g.31167839del , CM000668.1:g.31167839del GRCh37
NC_000006.10:g.31275818del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2180del
ENST00000414008.2:n.169del
ENST00000424675.1:c.44+1881del
NR_026791.1:n.123+2180del