Canonical Allele Identifier: CA5634171

Gene: HOGA1

Linked Data

• dbSNP Id: rs770323914
• ExAC: 10:99359609 C / G
• gnomAD v2: 10-99359609-C-G
• gnomAD v4: 10-97599852-C-G
• MyVariant Identifiers: chr10:g.99359609C>G (hg19) ; chr10:g.97599852C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599852C>G , CM000672.2:g.97599852C>G	GRCh38
NC_000010.10:g.99359609C>G , CM000672.1:g.99359609C>G	GRCh37
NC_000010.9:g.99349599C>G	NCBI36
NG_027922.1:g.20508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.603+38C>G MANE Select	ENSP00000359680.4:n.603+38C>G
ENST00000370642.4:c.13+38C>G
ENST00000370646.8:c.603+38C>G	ENSP00000359680.4:n.603+38C>G
ENST00000370647.8:c.212-2005C>G	ENSP00000359681.4:n.212-2005C>G
ENST00000370649.3:c.212-2005C>G	ENSP00000359683.3:n.212-2005C>G
ENST00000465608.1:n.1485C>G
NM_001134670.1:c.212-2005C>G	NP_001128142.1:n.212-2005C>G
NM_138413.3:c.603+38C>G	NP_612422.2:n.603+38C>G
NM_138413.4:c.603+38C>G MANE Select	NP_612422.2:n.603+38C>G
NM_001134670.2:c.212-2005C>G	NP_001128142.1:n.212-2005C>G