Canonical Allele Identifier: CA1087424323
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1779825156
gnomAD v3: 6-31200161-A-G
gnomAD v4: 6-31200161-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200161A>G , CM000668.2:g.31200161A>G GRCh38
NC_000006.11:g.31167938A>G , CM000668.1:g.31167938A>G GRCh37
NC_000006.10:g.31275917A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2211A>G
ENST00000414008.2:n.268A>G
ENST00000424675.1:c.44+1980A>G
NR_026791.1:n.124-2211A>G