Canonical Allele Identifier: CA9080723
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs529514617
gnomAD v2: 19-3595735-C-G
gnomAD v3: 19-3595737-C-G
gnomAD v4: 19-3595737-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595737C>G , CM000681.2:g.3595737C>G GRCh38
NC_000019.9:g.3595735C>G , CM000681.1:g.3595735C>G GRCh37
NC_000019.8:g.3546735C>G NCBI36
NG_013363.1:g.16097G>C , LRG_578:g.16097G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.983G>C MANE Select ENSP00000364336.4:p.Arg328Thr
ENST00000375190.8:c.983G>C ENSP00000364336.3:p.Arg328Thr
ENST00000411851.3:c.983G>C ENSP00000393333.2:p.Arg328Thr
ENST00000589966.1:c.594G>C ENSP00000468145.1:p.Gln198His
NM_001060.5:c.983G>C , LRG_578t1:c.983G>C NP_001051.1:p.Arg328Thr
NM_201636.2:c.983G>C NP_963998.2:p.Arg328Thr
XM_011528214.1:c.983G>C XP_011526516.1:p.Arg328Thr
XM_011528214.2:c.983G>C XP_011526516.1:p.Arg328Thr
NM_001060.6:c.983G>C MANE Select NP_001051.1:p.Arg328Thr
NM_201636.3:c.983G>C NP_963998.2:p.Arg328Thr