Canonical Allele Identifier: CA449627432
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200165-G-T
MyVariant Identifiers: chr6:g.31167942G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200165G>T , CM000668.2:g.31200165G>T GRCh38
NC_000006.11:g.31167942G>T , CM000668.1:g.31167942G>T GRCh37
NC_000006.10:g.31275921G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2207G>T
ENST00000414008.2:n.272G>T
ENST00000424675.1:c.44+1984G>T
NR_026791.1:n.124-2207G>T