Canonical Allele Identifier: CA343107053
Gene: TBX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 488619
ClinVar RCV Id: RCV000578226
dbSNP Id: rs1553289042
MyVariant Identifiers: chr1:g.168262481C>T (hg19) chr1:g.168293243C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293243C>T , CM000663.2:g.168293243C>T GRCh38
NC_000001.10:g.168262481C>T , CM000663.1:g.168262481C>T GRCh37
NC_000001.9:g.166529105C>T NCBI36
NG_008244.1:g.17204C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.568C>T MANE Select ENSP00000356795.3:p.Gln190Ter
ENST00000367821.7:c.568C>T ENSP00000356795.3:p.Gln190Ter
ENST00000431969.5:c.365C>T
NM_005149.2:c.568C>T NP_005140.1:p.Gln190Ter
NM_005149.3:c.568C>T MANE Select NP_005140.1:p.Gln190Ter
Search 100 bp 5'
Search 100 bp 3'