Canonical Allele Identifier: CA421716416
Gene: TBX19 HGNC NCBI

Linked Data

gnomAD v4: 1-168293254-C-G
MyVariant Identifiers: chr1:g.168262492C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293254C>G , CM000663.2:g.168293254C>G GRCh38
NC_000001.10:g.168262492C>G , CM000663.1:g.168262492C>G GRCh37
NC_000001.9:g.166529116C>G NCBI36
NG_008244.1:g.17215C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.579C>G MANE Select ENSP00000356795.3:p.Ala193=
ENST00000367821.7:c.579C>G ENSP00000356795.3:p.Ala193=
ENST00000431969.5:c.376C>G
NM_005149.2:c.579C>G NP_005140.1:p.Ala193=
NM_005149.3:c.579C>G MANE Select NP_005140.1:p.Ala193=
Search 100 bp 5'
Search 100 bp 3'