Canonical Allele Identifier: CA1008885403
Gene: TBX19 HGNC NCBI

Linked Data

dbSNP Id: rs1648928552
gnomAD v3: 1-168291146-G-A
gnomAD v4: 1-168291146-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168291146G>A , CM000663.2:g.168291146G>A GRCh38
NC_000001.10:g.168260384G>A , CM000663.1:g.168260384G>A GRCh37
NC_000001.9:g.166527008G>A NCBI36
NG_008244.1:g.15107G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.204-14G>A MANE Select ENSP00000356795.3:n.204-14G>A
ENST00000367821.7:c.204-14G>A ENSP00000356795.3:n.204-14G>A
NM_005149.2:c.204-14G>A NP_005140.1:n.204-14G>A
NM_005149.3:c.204-14G>A MANE Select NP_005140.1:n.204-14G>A
Search 100 bp 5'
Search 100 bp 3'