Canonical Allele Identifier: CA2677946824

Gene: HCG27

Linked Data

• gnomAD v4: 6-31200155-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31200155T>C , CM000668.2:g.31200155T>C	GRCh38
NC_000006.11:g.31167932T>C , CM000668.1:g.31167932T>C	GRCh37
NC_000006.10:g.31275911T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383331.4:c.124-2217T>C
ENST00000414008.2:n.262T>C
ENST00000424675.1:c.44+1974T>C
NR_026791.1:n.124-2217T>C