Canonical Allele Identifier: CA2677946789
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200073-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200073C>A , CM000668.2:g.31200073C>A GRCh38
NC_000006.11:g.31167850C>A , CM000668.1:g.31167850C>A GRCh37
NC_000006.10:g.31275829C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2191C>A
ENST00000414008.2:n.180C>A
ENST00000424675.1:c.44+1892C>A
NR_026791.1:n.123+2191C>A