Canonical Allele Identifier: CA449627531
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1247509692
gnomAD v3: 6-31200173-A-T
gnomAD v4: 6-31200173-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200173A>T , CM000668.2:g.31200173A>T GRCh38
NC_000006.11:g.31167950A>T , CM000668.1:g.31167950A>T GRCh37
NC_000006.10:g.31275929A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.124-2199A>T
ENST00000414008.2:n.280A>T
ENST00000424675.1:c.44+1992A>T
NR_026791.1:n.124-2199A>T