Canonical Allele Identifier: CA1205614316
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs1649007603

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293505A>G , CM000663.2:g.168293505A>G GRCh38
NC_000001.10:g.168262743A>G , CM000663.1:g.168262743A>G GRCh37
NC_000001.9:g.166529367A>G NCBI36
NG_008244.1:g.17466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+227A>G MANE Select ENSP00000356795.3:n.603+227A>G
ENST00000367821.7:c.603+227A>G ENSP00000356795.3:n.603+227A>G
ENST00000431969.5:c.400+227A>G
NM_005149.2:c.603+227A>G NP_005140.1:n.603+227A>G
NM_005149.3:c.603+227A>G MANE Select NP_005140.1:n.603+227A>G