Canonical Allele Identifier: CA389466563
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132405G>T (hg19) chr14:g.36663200G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663200G>T , CM000676.2:g.36663200G>T GRCh38
NC_000014.8:g.37132405G>T , CM000676.1:g.37132405G>T GRCh37
NC_000014.7:g.36202156G>T NCBI36
NG_013357.1:g.10633G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.308G>T MANE Select ENSP00000355245.6:p.Arg103Leu
ENST00000361487.6:c.308G>T ENSP00000355245.6:p.Arg103Leu
ENST00000402703.6:c.308G>T ENSP00000384817.2:p.Arg103Leu
ENST00000554201.1:c.-254G>T ENSP00000450434.1:n.-254G>T
NM_006194.3:c.308G>T NP_006185.1:p.Arg103Leu
NM_001372076.1:c.308G>T MANE Select NP_001359005.1:p.Arg103Leu
NM_006194.4:c.308G>T NP_006185.1:p.Arg103Leu
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