Canonical Allele Identifier: CA449627460
Gene: HCG27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31167946T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200169T>A , CM000668.2:g.31200169T>A GRCh38
NC_000006.11:g.31167946T>A , CM000668.1:g.31167946T>A GRCh37
NC_000006.10:g.31275925T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2203T>A
ENST00000414008.2:n.276T>A
ENST00000424675.1:c.44+1988T>A
NR_026791.1:n.124-2203T>A