Canonical Allele Identifier: CA212682968
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs968509662
MyVariant Identifiers: chr10:g.99371113A>C (hg19) chr10:g.97611356A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611356A>C , CM000672.2:g.97611356A>C GRCh38
NC_000010.10:g.99371113A>C , CM000672.1:g.99371113A>C GRCh37
NC_000010.9:g.99361103A>C NCBI36
NG_027922.1:g.32012A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.835-154A>C MANE Select ENSP00000359680.4:n.835-154A>C
ENST00000370646.8:c.835-154A>C ENSP00000359680.4:n.835-154A>C
ENST00000370647.8:c.346-154A>C ENSP00000359681.4:n.346-154A>C
ENST00000370649.3:c.345+9366A>C ENSP00000359683.3:n.345+9366A>C
NM_001134670.1:c.346-154A>C NP_001128142.1:n.346-154A>C
NM_138413.3:c.835-154A>C NP_612422.2:n.835-154A>C
NM_138413.4:c.835-154A>C MANE Select NP_612422.2:n.835-154A>C
NM_001134670.2:c.346-154A>C NP_001128142.1:n.346-154A>C
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