Canonical Allele Identifier: CA1205614265
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs10800350
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293386A>C , CM000663.2:g.168293386A>C GRCh38
NC_000001.10:g.168262624A>C , CM000663.1:g.168262624A>C GRCh37
NC_000001.9:g.166529248A>C NCBI36
NG_008244.1:g.17347A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+108A>C MANE Select ENSP00000356795.3:n.603+108A>C
ENST00000367821.7:c.603+108A>C ENSP00000356795.3:n.603+108A>C
ENST00000431969.5:c.400+108A>C
NM_005149.2:c.603+108A>C NP_005140.1:n.603+108A>C
NM_005149.3:c.603+108A>C MANE Select NP_005140.1:n.603+108A>C
Search 100 bp 5'
Search 100 bp 3'