Canonical Allele Identifier: CA2576567932
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595347C>G , CM000681.2:g.3595347C>G GRCh38
NC_000019.9:g.3595345C>G , CM000681.1:g.3595345C>G GRCh37
NC_000019.8:g.3546345C>G NCBI36
NG_013363.1:g.16487G>C , LRG_578:g.16487G>C
NG_031943.1:g.14777C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*341G>C MANE Select ENSP00000364336.4:n.*341G>C
ENST00000375190.8:c.*341G>C ENSP00000364336.3:n.*341G>C
ENST00000411851.3:c.984-271G>C ENSP00000393333.2:n.984-271G>C
ENST00000589966.1:c.*204G>C ENSP00000468145.1:n.*204G>C
NM_001060.5:c.*341G>C , LRG_578t1:c.*341G>C NP_001051.1:n.*341G>C
NM_201636.2:c.984-271G>C NP_963998.2:n.984-271G>C
NM_001060.6:c.*341G>C MANE Select NP_001051.1:n.*341G>C
NM_201636.3:c.984-271G>C NP_963998.2:n.984-271G>C