Canonical Allele Identifier: CA1143730291
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293101G= , CM000663.2:g.168293101G= GRCh38
NC_000001.10:g.168262339G= , CM000663.1:g.168262339G= GRCh37
NC_000001.9:g.166528963G= NCBI36
NG_008244.1:g.17062G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-43G= MANE Select ENSP00000356795.3:n.469-43G=
ENST00000367821.7:c.469-43G= ENSP00000356795.3:n.469-43G=
ENST00000431969.5:c.266-43G=
NM_005149.2:c.469-43G= NP_005140.1:n.469-43G=
NM_005149.3:c.469-43G= MANE Select NP_005140.1:n.469-43G=