Canonical Allele Identifier: CA631504256
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs1568281512
gnomAD v2: 19-3595375-T-C
gnomAD v3: 19-3595377-T-C
gnomAD v4: 19-3595377-T-C
MyVariant Identifiers: chr19:g.3595375_3595376delinsCA (hg19) chr19:g.3595377_3595378delinsCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595377T>C , CM000681.2:g.3595377T>C GRCh38
NC_000019.9:g.3595375T>C , CM000681.1:g.3595375T>C GRCh37
NC_000019.8:g.3546375T>C NCBI36
NG_013363.1:g.16457A>G , LRG_578:g.16457A>G
NG_031943.1:g.14807T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*311A>G MANE Select ENSP00000364336.4:n.*311A>G
ENST00000375190.8:c.*311A>G ENSP00000364336.3:n.*311A>G
ENST00000411851.3:c.984-301A>G ENSP00000393333.2:n.984-301A>G
ENST00000589966.1:c.*174A>G ENSP00000468145.1:n.*174A>G
NM_001060.5:c.*311A>G , LRG_578t1:c.*311A>G NP_001051.1:n.*311A>G
NM_201636.2:c.984-301A>G NP_963998.2:n.984-301A>G
NM_001060.6:c.*311A>G MANE Select NP_001051.1:n.*311A>G
NM_201636.3:c.984-301A>G NP_963998.2:n.984-301A>G
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