Canonical Allele Identifier: CA136833615

Gene: HCG27

Linked Data

• dbSNP Id: rs983682309
• MyVariant Identifiers: chr6:g.31167872A>C (hg19) ; chr6:g.31200095A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31200095A>C , CM000668.2:g.31200095A>C	GRCh38
NC_000006.11:g.31167872A>C , CM000668.1:g.31167872A>C	GRCh37
NC_000006.10:g.31275851A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383331.4:c.123+2213A>C
ENST00000414008.2:n.202A>C
ENST00000424675.1:c.44+1914A>C
NR_026791.1:n.123+2213A>C