Canonical Allele Identifier: CA421715202
Gene: TBX19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.168260464G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291226G>C , CM000663.2:g.168291226G>C GRCh38
NC_000001.10:g.168260464G>C , CM000663.1:g.168260464G>C GRCh37
NC_000001.9:g.166527088G>C NCBI36
NG_008244.1:g.15187G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.270G>C MANE Select ENSP00000356795.3:p.Leu90=
ENST00000367821.7:c.270G>C ENSP00000356795.3:p.Leu90=
ENST00000431969.5:c.67G>C
NM_005149.2:c.270G>C NP_005140.1:p.Leu90=
NM_005149.3:c.270G>C MANE Select NP_005140.1:p.Leu90=