Canonical Allele Identifier: CA992743574
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032579355
gnomAD v3: 19-3595443-G-GA
gnomAD v4: 19-3595443-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595444dup , CM000681.2:g.3595444dup GRCh38
NC_000019.9:g.3595442dup , CM000681.1:g.3595442dup GRCh37
NC_000019.8:g.3546442dup NCBI36
NG_013363.1:g.16390dup , LRG_578:g.16390dup
NG_031943.1:g.14874dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*244dup MANE Select ENSP00000364336.4:n.*244dup
ENST00000375190.8:c.*244dup ENSP00000364336.3:n.*244dup
ENST00000411851.3:c.983+293dup ENSP00000393333.2:n.983+293dup
ENST00000589966.1:c.*107dup ENSP00000468145.1:n.*107dup
NM_001060.5:c.*244dup , LRG_578t1:c.*244dup NP_001051.1:n.*244dup
NM_201636.2:c.983+293dup NP_963998.2:n.983+293dup
NM_001060.6:c.*244dup MANE Select NP_001051.1:n.*244dup
NM_201636.3:c.983+293dup NP_963998.2:n.983+293dup
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