Canonical Allele Identifier: CA136833638
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1000131027

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200163C>T , CM000668.2:g.31200163C>T GRCh38
NC_000006.11:g.31167940C>T , CM000668.1:g.31167940C>T GRCh37
NC_000006.10:g.31275919C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2209C>T
ENST00000414008.2:n.270C>T
ENST00000424675.1:c.44+1982C>T
NR_026791.1:n.124-2209C>T