Canonical Allele Identifier: CA1205613325
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291221C= , CM000663.2:g.168291221C= GRCh38
NC_000001.10:g.168260459C= , CM000663.1:g.168260459C= GRCh37
NC_000001.9:g.166527083C= NCBI36
NG_008244.1:g.15182C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.265C= MANE Select ENSP00000356795.3:p.Leu89=
ENST00000367821.7:c.265C= ENSP00000356795.3:p.Leu89=
ENST00000431969.5:c.62C=
NM_005149.2:c.265C= NP_005140.1:p.Leu89=
NM_005149.3:c.265C= MANE Select NP_005140.1:p.Leu89=