Canonical Allele Identifier: CA2584493671
Gene: TBXA2R HGNC NCBI

Linked Data

gnomAD v4: 19-3595408-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595408T>C , CM000681.2:g.3595408T>C GRCh38
NC_000019.9:g.3595406T>C , CM000681.1:g.3595406T>C GRCh37
NC_000019.8:g.3546406T>C NCBI36
NG_013363.1:g.16426A>G , LRG_578:g.16426A>G
NG_031943.1:g.14838T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*280A>G MANE Select ENSP00000364336.4:n.*280A>G
ENST00000375190.8:c.*280A>G ENSP00000364336.3:n.*280A>G
ENST00000411851.3:c.983+329A>G ENSP00000393333.2:n.983+329A>G
ENST00000589966.1:c.*143A>G ENSP00000468145.1:n.*143A>G
NM_001060.5:c.*280A>G , LRG_578t1:c.*280A>G NP_001051.1:n.*280A>G
NM_201636.2:c.983+329A>G NP_963998.2:n.983+329A>G
NM_001060.6:c.*280A>G MANE Select NP_001051.1:n.*280A>G
NM_201636.3:c.983+329A>G NP_963998.2:n.983+329A>G
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