Canonical Allele Identifier: CA136833633
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs138823893
gnomAD v2: 6-31167935-A-G
gnomAD v3: 6-31200158-A-G
gnomAD v4: 6-31200158-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200158A>G , CM000668.2:g.31200158A>G GRCh38
NC_000006.11:g.31167935A>G , CM000668.1:g.31167935A>G GRCh37
NC_000006.10:g.31275914A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2214A>G
ENST00000414008.2:n.265A>G
ENST00000424675.1:c.44+1977A>G
NR_026791.1:n.124-2214A>G