Canonical Allele Identifier: CA2318945613
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs570239890
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595397C>T , CM000681.2:g.3595397C>T GRCh38
NC_000019.9:g.3595395C>T , CM000681.1:g.3595395C>T GRCh37
NC_000019.8:g.3546395C>T NCBI36
NG_013363.1:g.16437G>A , LRG_578:g.16437G>A
NG_031943.1:g.14827C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*291G>A MANE Select ENSP00000364336.4:n.*291G>A
ENST00000375190.8:c.*291G>A ENSP00000364336.3:n.*291G>A
ENST00000411851.3:c.984-321G>A ENSP00000393333.2:n.984-321G>A
ENST00000589966.1:c.*154G>A ENSP00000468145.1:n.*154G>A
NM_001060.5:c.*291G>A , LRG_578t1:c.*291G>A NP_001051.1:n.*291G>A
NM_201636.2:c.984-321G>A NP_963998.2:n.984-321G>A
NM_001060.6:c.*291G>A MANE Select NP_001051.1:n.*291G>A
NM_201636.3:c.984-321G>A NP_963998.2:n.984-321G>A
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