Canonical Allele Identifier: CA5634200
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2192715
ClinVar RCV Id: RCV002607618
dbSNP Id: rs753833846
ExAC: 10:99359935 G / T
gnomAD v2: 10-99359935-G-T
gnomAD v4: 10-97600178-G-T
MyVariant Identifiers: chr10:g.99359935G>T (hg19) chr10:g.97600178G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97600178G>T , CM000672.2:g.97600178G>T GRCh38
NC_000010.10:g.99359935G>T , CM000672.1:g.99359935G>T GRCh37
NC_000010.9:g.99349925G>T NCBI36
NG_027922.1:g.20834G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.700+15G>T MANE Select ENSP00000359680.4:n.700+15G>T
ENST00000370642.4:c.110+15G>T
ENST00000370646.8:c.700+15G>T ENSP00000359680.4:n.700+15G>T
ENST00000370647.8:c.212-1679G>T ENSP00000359681.4:n.212-1679G>T
ENST00000370649.3:c.212-1679G>T ENSP00000359683.3:n.212-1679G>T
ENST00000465608.1:n.1811G>T
NM_001134670.1:c.212-1679G>T NP_001128142.1:n.212-1679G>T
NM_138413.3:c.700+15G>T NP_612422.2:n.700+15G>T
NM_138413.4:c.700+15G>T MANE Select NP_612422.2:n.700+15G>T
NM_001134670.2:c.212-1679G>T NP_001128142.1:n.212-1679G>T
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