Canonical Allele Identifier: CA2746547405
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293372T>G , CM000663.2:g.168293372T>G GRCh38
NC_000001.10:g.168262610T>G , CM000663.1:g.168262610T>G GRCh37
NC_000001.9:g.166529234T>G NCBI36
NG_008244.1:g.17333T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+94T>G MANE Select ENSP00000356795.3:n.603+94T>G
ENST00000367821.7:c.603+94T>G ENSP00000356795.3:n.603+94T>G
ENST00000431969.5:c.400+94T>G
NM_005149.2:c.603+94T>G NP_005140.1:n.603+94T>G
NM_005149.3:c.603+94T>G MANE Select NP_005140.1:n.603+94T>G