Canonical Allele Identifier: CA389466539
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132396G>C (hg19) chr14:g.36663191G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663191G>C , CM000676.2:g.36663191G>C GRCh38
NC_000014.8:g.37132396G>C , CM000676.1:g.37132396G>C GRCh37
NC_000014.7:g.36202147G>C NCBI36
NG_013357.1:g.10624G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.299G>C MANE Select ENSP00000355245.6:p.Trp100Ser
ENST00000361487.6:c.299G>C ENSP00000355245.6:p.Trp100Ser
ENST00000402703.6:c.299G>C ENSP00000384817.2:p.Trp100Ser
ENST00000554201.1:c.-263G>C ENSP00000450434.1:n.-263G>C
NM_006194.3:c.299G>C NP_006185.1:p.Trp100Ser
NM_001372076.1:c.299G>C MANE Select NP_001359005.1:p.Trp100Ser
NM_006194.4:c.299G>C NP_006185.1:p.Trp100Ser
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