Canonical Allele Identifier: CA670419904

Gene: HOGA1

Linked Data

• dbSNP Id: rs1308549446
• gnomAD v3: 10-97600191-C-T
• gnomAD v4: 10-97600191-C-T
• MyVariant Identifiers: chr10:g.99359948C>T (hg19) ; chr10:g.97600191C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600191C>T , CM000672.2:g.97600191C>T	GRCh38
NC_000010.10:g.99359948C>T , CM000672.1:g.99359948C>T	GRCh37
NC_000010.9:g.99349938C>T	NCBI36
NG_027922.1:g.20847C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.700+28C>T MANE Select	ENSP00000359680.4:n.700+28C>T
ENST00000370642.4:c.110+28C>T
ENST00000370646.8:c.700+28C>T	ENSP00000359680.4:n.700+28C>T
ENST00000370647.8:c.212-1666C>T	ENSP00000359681.4:n.212-1666C>T
ENST00000370649.3:c.212-1666C>T	ENSP00000359683.3:n.212-1666C>T
ENST00000465608.1:n.1824C>T
NM_001134670.1:c.212-1666C>T	NP_001128142.1:n.212-1666C>T
NM_138413.3:c.700+28C>T	NP_612422.2:n.700+28C>T
NM_138413.4:c.700+28C>T MANE Select	NP_612422.2:n.700+28C>T
NM_001134670.2:c.212-1666C>T	NP_001128142.1:n.212-1666C>T