Canonical Allele Identifier: CA389466352
Gene: PAX9 HGNC NCBI

Linked Data

gnomAD v4: 14-36663104-T-C
MyVariant Identifiers: chr14:g.37132309T>C (hg19) chr14:g.36663104T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663104T>C , CM000676.2:g.36663104T>C GRCh38
NC_000014.8:g.37132309T>C , CM000676.1:g.37132309T>C GRCh37
NC_000014.7:g.36202060T>C NCBI36
NG_013357.1:g.10537T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.212T>C MANE Select ENSP00000355245.6:p.Ile71Thr
ENST00000555639.2:c.212T>C ENSP00000501203.1:p.Ile71Thr
ENST00000361487.6:c.212T>C ENSP00000355245.6:p.Ile71Thr
ENST00000402703.6:c.212T>C ENSP00000384817.2:p.Ile71Thr
ENST00000554201.1:c.-350T>C ENSP00000450434.1:n.-350T>C
ENST00000555639.1:n.514T>C
NM_006194.3:c.212T>C NP_006185.1:p.Ile71Thr
NM_001372076.1:c.212T>C MANE Select NP_001359005.1:p.Ile71Thr
NM_006194.4:c.212T>C NP_006185.1:p.Ile71Thr
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