Canonical Allele Identifier: CA2677946825
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200159-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200159C>T , CM000668.2:g.31200159C>T GRCh38
NC_000006.11:g.31167936C>T , CM000668.1:g.31167936C>T GRCh37
NC_000006.10:g.31275915C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2213C>T
ENST00000414008.2:n.266C>T
ENST00000424675.1:c.44+1978C>T
NR_026791.1:n.124-2213C>T