Canonical Allele Identifier: CA449627591

Gene: HCG27

Linked Data

• dbSNP Id: rs1341464645
• MyVariant Identifiers: chr6:g.31167956G>C (hg19) ; chr6:g.31200179G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31200179G>C , CM000668.2:g.31200179G>C	GRCh38
NC_000006.11:g.31167956G>C , CM000668.1:g.31167956G>C	GRCh37
NC_000006.10:g.31275935G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383331.4:c.124-2193G>C
ENST00000414008.2:n.286G>C
ENST00000424675.1:c.44+1998G>C
NR_026791.1:n.124-2193G>C