Canonical Allele Identifier: CA449627448
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1371108773
gnomAD v2: 6-31167945-G-A
gnomAD v3: 6-31200168-G-A
gnomAD v4: 6-31200168-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200168G>A , CM000668.2:g.31200168G>A GRCh38
NC_000006.11:g.31167945G>A , CM000668.1:g.31167945G>A GRCh37
NC_000006.10:g.31275924G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2204G>A
ENST00000414008.2:n.275G>A
ENST00000424675.1:c.44+1987G>A
NR_026791.1:n.124-2204G>A