Canonical Allele Identifier: CA2677946767
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200005-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200005A>G , CM000668.2:g.31200005A>G GRCh38
NC_000006.11:g.31167782A>G , CM000668.1:g.31167782A>G GRCh37
NC_000006.10:g.31275761A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2123A>G
ENST00000414008.2:n.112A>G
ENST00000424675.1:c.44+1824A>G
NR_026791.1:n.123+2123A>G