Canonical Allele Identifier: CA2740195851
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293130T>C , CM000663.2:g.168293130T>C GRCh38
NC_000001.10:g.168262368T>C , CM000663.1:g.168262368T>C GRCh37
NC_000001.9:g.166528992T>C NCBI36
NG_008244.1:g.17091T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.469-14T>C MANE Select ENSP00000356795.3:n.469-14T>C
ENST00000367821.7:c.469-14T>C ENSP00000356795.3:n.469-14T>C
ENST00000431969.5:c.266-14T>C
NM_005149.2:c.469-14T>C NP_005140.1:n.469-14T>C
NM_005149.3:c.469-14T>C MANE Select NP_005140.1:n.469-14T>C