Canonical Allele Identifier: CA449627491
Gene: HCG27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31167947A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200170A>C , CM000668.2:g.31200170A>C GRCh38
NC_000006.11:g.31167947A>C , CM000668.1:g.31167947A>C GRCh37
NC_000006.10:g.31275926A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2202A>C
ENST00000414008.2:n.277A>C
ENST00000424675.1:c.44+1989A>C
NR_026791.1:n.124-2202A>C