Canonical Allele Identifier: CA485930898
Gene: PAX9 HGNC NCBI

Linked Data

dbSNP Id: rs1881369184
gnomAD v4: 14-36663480-C-T
MyVariant Identifiers: chr14:g.37132685C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663480C>T , CM000676.2:g.36663480C>T GRCh38
NC_000014.8:g.37132685C>T , CM000676.1:g.37132685C>T GRCh37
NC_000014.7:g.36202436C>T NCBI36
NG_013357.1:g.10913C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.588C>T MANE Select ENSP00000355245.6:p.His196=
ENST00000361487.6:c.588C>T ENSP00000355245.6:p.His196=
ENST00000402703.6:c.588C>T ENSP00000384817.2:p.His196=
ENST00000554201.1:c.27C>T ENSP00000450434.1:p.His9=
NM_006194.3:c.588C>T NP_006185.1:p.His196=
NM_001372076.1:c.588C>T MANE Select NP_001359005.1:p.His196=
NM_006194.4:c.588C>T NP_006185.1:p.His196=
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