Canonical Allele Identifier: CA2677946760
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31199982-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31199982G>T , CM000668.2:g.31199982G>T GRCh38
NC_000006.11:g.31167759G>T , CM000668.1:g.31167759G>T GRCh37
NC_000006.10:g.31275738G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2100G>T
ENST00000414008.2:n.89G>T
ENST00000424675.1:c.44+1801G>T
NR_026791.1:n.123+2100G>T
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