Canonical Allele Identifier: CA2584493798
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1357790203
gnomAD v4: 19-3595605-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595605T>C , CM000681.2:g.3595605T>C GRCh38
NC_000019.9:g.3595603T>C , CM000681.1:g.3595603T>C GRCh37
NC_000019.8:g.3546603T>C NCBI36
NG_013363.1:g.16229A>G , LRG_578:g.16229A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*83A>G MANE Select ENSP00000364336.4:n.*83A>G
ENST00000375190.8:c.*83A>G ENSP00000364336.3:n.*83A>G
ENST00000411851.3:c.983+132A>G ENSP00000393333.2:n.983+132A>G
ENST00000589966.1:c.726A>G ENSP00000468145.1:p.Ser242=
NM_001060.5:c.*83A>G , LRG_578t1:c.*83A>G NP_001051.1:n.*83A>G
NM_201636.2:c.983+132A>G NP_963998.2:n.983+132A>G
XM_011528214.1:c.*83A>G XP_011526516.1:n.*83A>G
XM_011528214.2:c.*83A>G XP_011526516.1:n.*83A>G
NM_001060.6:c.*83A>G MANE Select NP_001051.1:n.*83A>G
NM_201636.3:c.983+132A>G NP_963998.2:n.983+132A>G