Canonical Allele Identifier: CA421715197
Gene: TBX19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.168260458C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291220C>A , CM000663.2:g.168291220C>A GRCh38
NC_000001.10:g.168260458C>A , CM000663.1:g.168260458C>A GRCh37
NC_000001.9:g.166527082C>A NCBI36
NG_008244.1:g.15181C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367821.8:c.264C>A MANE Select ENSP00000356795.3:p.Ser88=
ENST00000367821.7:c.264C>A ENSP00000356795.3:p.Ser88=
ENST00000431969.5:c.61C>A
NM_005149.2:c.264C>A NP_005140.1:p.Ser88=
NM_005149.3:c.264C>A MANE Select NP_005140.1:p.Ser88=
Search 100 bp 5'
Search 100 bp 3'