Canonical Allele Identifier: CA992743553
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1599868612
gnomAD v3: 19-3595395-T-G
gnomAD v4: 19-3595395-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595395T>G , CM000681.2:g.3595395T>G GRCh38
NC_000019.9:g.3595393T>G , CM000681.1:g.3595393T>G GRCh37
NC_000019.8:g.3546393T>G NCBI36
NG_013363.1:g.16439A>C , LRG_578:g.16439A>C
NG_031943.1:g.14825T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*293A>C MANE Select ENSP00000364336.4:n.*293A>C
ENST00000375190.8:c.*293A>C ENSP00000364336.3:n.*293A>C
ENST00000411851.3:c.984-319A>C ENSP00000393333.2:n.984-319A>C
ENST00000589966.1:c.*156A>C ENSP00000468145.1:n.*156A>C
NM_001060.5:c.*293A>C , LRG_578t1:c.*293A>C NP_001051.1:n.*293A>C
NM_201636.2:c.984-319A>C NP_963998.2:n.984-319A>C
NM_001060.6:c.*293A>C MANE Select NP_001051.1:n.*293A>C
NM_201636.3:c.984-319A>C NP_963998.2:n.984-319A>C
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