Canonical Allele Identifier: CA389466957
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132590C>T (hg19) chr14:g.36663385C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663385C>T , CM000676.2:g.36663385C>T GRCh38
NC_000014.8:g.37132590C>T , CM000676.1:g.37132590C>T GRCh37
NC_000014.7:g.36202341C>T NCBI36
NG_013357.1:g.10818C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.493C>T MANE Select ENSP00000355245.6:p.Pro165Ser
ENST00000361487.6:c.493C>T ENSP00000355245.6:p.Pro165Ser
ENST00000402703.6:c.493C>T ENSP00000384817.2:p.Pro165Ser
ENST00000554201.1:c.-69C>T ENSP00000450434.1:n.-69C>T
NM_006194.3:c.493C>T NP_006185.1:p.Pro165Ser
NM_001372076.1:c.493C>T MANE Select NP_001359005.1:p.Pro165Ser
NM_006194.4:c.493C>T NP_006185.1:p.Pro165Ser
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