Canonical Allele Identifier: CA449627425
Gene: HCG27 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31167942G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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