Canonical Allele Identifier: CA1087424278
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1582147895
gnomAD v3: 6-31200088-G-A
gnomAD v4: 6-31200088-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200088G>A , CM000668.2:g.31200088G>A GRCh38
NC_000006.11:g.31167865G>A , CM000668.1:g.31167865G>A GRCh37
NC_000006.10:g.31275844G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2206G>A
ENST00000414008.2:n.195G>A
ENST00000424675.1:c.44+1907G>A
NR_026791.1:n.123+2206G>A