Canonical Allele Identifier: CA2677946766
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200002-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200002G>T , CM000668.2:g.31200002G>T GRCh38
NC_000006.11:g.31167779G>T , CM000668.1:g.31167779G>T GRCh37
NC_000006.10:g.31275758G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2120G>T
ENST00000414008.2:n.109G>T
ENST00000424675.1:c.44+1821G>T
NR_026791.1:n.123+2120G>T
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