Canonical Allele Identifier: CA403330565
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595799C>G , CM000681.2:g.3595799C>G GRCh38
NC_000019.9:g.3595797C>G , CM000681.1:g.3595797C>G GRCh37
NC_000019.8:g.3546797C>G NCBI36
NG_013363.1:g.16035G>C , LRG_578:g.16035G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.921G>C MANE Select ENSP00000364336.4:p.Val307=
ENST00000375190.8:c.921G>C ENSP00000364336.3:p.Val307=
ENST00000411851.3:c.921G>C ENSP00000393333.2:p.Val307=
ENST00000589966.1:c.532G>C ENSP00000468145.1:p.Val178Leu
NM_001060.5:c.921G>C , LRG_578t1:c.921G>C NP_001051.1:p.Val307=
NM_201636.2:c.921G>C NP_963998.2:p.Val307=
XM_011528214.1:c.921G>C XP_011526516.1:p.Val307=
XM_011528214.2:c.921G>C XP_011526516.1:p.Val307=
NM_001060.6:c.921G>C MANE Select NP_001051.1:p.Val307=
NM_201636.3:c.921G>C NP_963998.2:p.Val307=