Canonical Allele Identifier: CA343106854
Gene: TBX19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.168262391A>C (hg19) chr1:g.168293153A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293153A>C , CM000663.2:g.168293153A>C GRCh38
NC_000001.10:g.168262391A>C , CM000663.1:g.168262391A>C GRCh37
NC_000001.9:g.166529015A>C NCBI36
NG_008244.1:g.17114A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.478A>C MANE Select ENSP00000356795.3:p.Asn160His
ENST00000367821.7:c.478A>C ENSP00000356795.3:p.Asn160His
ENST00000431969.5:c.275A>C
NM_005149.2:c.478A>C NP_005140.1:p.Asn160His
NM_005149.3:c.478A>C MANE Select NP_005140.1:p.Asn160His
Search 100 bp 5'
Search 100 bp 3'