Canonical Allele Identifier: CA421716427
Gene: TBX19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.168262504T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293266T>C , CM000663.2:g.168293266T>C GRCh38
NC_000001.10:g.168262504T>C , CM000663.1:g.168262504T>C GRCh37
NC_000001.9:g.166529128T>C NCBI36
NG_008244.1:g.17227T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.591T>C MANE Select ENSP00000356795.3:p.Tyr197=
ENST00000367821.7:c.591T>C ENSP00000356795.3:p.Tyr197=
ENST00000431969.5:c.388T>C
NM_005149.2:c.591T>C NP_005140.1:p.Tyr197=
NM_005149.3:c.591T>C MANE Select NP_005140.1:p.Tyr197=
Search 100 bp 5'
Search 100 bp 3'