Canonical Allele Identifier: CA1087424317
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1779824650
gnomAD v3: 6-31200153-A-C
gnomAD v4: 6-31200153-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200153A>C , CM000668.2:g.31200153A>C GRCh38
NC_000006.11:g.31167930A>C , CM000668.1:g.31167930A>C GRCh37
NC_000006.10:g.31275909A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2219A>C
ENST00000414008.2:n.260A>C
ENST00000424675.1:c.44+1972A>C
NR_026791.1:n.124-2219A>C