Canonical Allele Identifier: CA2677946788
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200072-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200072G>T , CM000668.2:g.31200072G>T GRCh38
NC_000006.11:g.31167849G>T , CM000668.1:g.31167849G>T GRCh37
NC_000006.10:g.31275828G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2190G>T
ENST00000414008.2:n.179G>T
ENST00000424675.1:c.44+1891G>T
NR_026791.1:n.123+2190G>T