Canonical Allele Identifier: CA136833595

Gene: HCG27

Linked Data

• dbSNP Id: rs1051452731
• MyVariant Identifiers: chr6:g.31167813T>C (hg19) ; chr6:g.31200036T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31200036T>C , CM000668.2:g.31200036T>C	GRCh38
NC_000006.11:g.31167813T>C , CM000668.1:g.31167813T>C	GRCh37
NC_000006.10:g.31275792T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383331.4:c.123+2154T>C
ENST00000414008.2:n.143T>C
ENST00000424675.1:c.44+1855T>C
NR_026791.1:n.123+2154T>C