Canonical Allele Identifier: CA343106958
Gene: TBX19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293201A>G , CM000663.2:g.168293201A>G GRCh38
NC_000001.10:g.168262439A>G , CM000663.1:g.168262439A>G GRCh37
NC_000001.9:g.166529063A>G NCBI36
NG_008244.1:g.17162A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.526A>G MANE Select ENSP00000356795.3:p.Ser176Gly
ENST00000367821.7:c.526A>G ENSP00000356795.3:p.Ser176Gly
ENST00000431969.5:c.323A>G
NM_005149.2:c.526A>G NP_005140.1:p.Ser176Gly
NM_005149.3:c.526A>G MANE Select NP_005140.1:p.Ser176Gly