Canonical Allele Identifier: CA421716424
Gene: TBX19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.168262501C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293263C>A , CM000663.2:g.168293263C>A GRCh38
NC_000001.10:g.168262501C>A , CM000663.1:g.168262501C>A GRCh37
NC_000001.9:g.166529125C>A NCBI36
NG_008244.1:g.17224C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.588C>A MANE Select ENSP00000356795.3:p.Ala196=
ENST00000367821.7:c.588C>A ENSP00000356795.3:p.Ala196=
ENST00000431969.5:c.385C>A
NM_005149.2:c.588C>A NP_005140.1:p.Ala196=
NM_005149.3:c.588C>A MANE Select NP_005140.1:p.Ala196=
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