Canonical Allele Identifier: CA136833605

Gene: HCG27

Linked Data

• dbSNP Id: rs964812739
• MyVariant Identifiers: chr6:g.31167837G>C (hg19) ; chr6:g.31200060G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31200060G>C , CM000668.2:g.31200060G>C	GRCh38
NC_000006.11:g.31167837G>C , CM000668.1:g.31167837G>C	GRCh37
NC_000006.10:g.31275816G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383331.4:c.123+2178G>C
ENST00000414008.2:n.167G>C
ENST00000424675.1:c.44+1879G>C
NR_026791.1:n.123+2178G>C