Canonical Allele Identifier: CA389467124
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663473C>G , CM000676.2:g.36663473C>G GRCh38
NC_000014.8:g.37132678C>G , CM000676.1:g.37132678C>G GRCh37
NC_000014.7:g.36202429C>G NCBI36
NG_013357.1:g.10906C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.581C>G MANE Select ENSP00000355245.6:p.Ser194Cys
ENST00000361487.6:c.581C>G ENSP00000355245.6:p.Ser194Cys
ENST00000402703.6:c.581C>G ENSP00000384817.2:p.Ser194Cys
ENST00000554201.1:c.20C>G ENSP00000450434.1:p.Ser7Cys
NM_006194.3:c.581C>G NP_006185.1:p.Ser194Cys
NM_001372076.1:c.581C>G MANE Select NP_001359005.1:p.Ser194Cys
NM_006194.4:c.581C>G NP_006185.1:p.Ser194Cys