Canonical Allele Identifier: CA486097933
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132376A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663171A>G , CM000676.2:g.36663171A>G GRCh38
NC_000014.8:g.37132376A>G , CM000676.1:g.37132376A>G GRCh37
NC_000014.7:g.36202127A>G NCBI36
NG_013357.1:g.10604A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.279A>G MANE Select ENSP00000355245.6:p.Arg93=
ENST00000361487.6:c.279A>G ENSP00000355245.6:p.Arg93=
ENST00000402703.6:c.279A>G ENSP00000384817.2:p.Arg93=
ENST00000554201.1:c.-283A>G ENSP00000450434.1:n.-283A>G
NM_006194.3:c.279A>G NP_006185.1:p.Arg93=
NM_001372076.1:c.279A>G MANE Select NP_001359005.1:p.Arg93=
NM_006194.4:c.279A>G NP_006185.1:p.Arg93=
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