Canonical Allele Identifier: CA403331265
Gene: TBXA2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595911A>C , CM000681.2:g.3595911A>C GRCh38
NC_000019.9:g.3595909A>C , CM000681.1:g.3595909A>C GRCh37
NC_000019.8:g.3546909A>C NCBI36
NG_013363.1:g.15923T>G , LRG_578:g.15923T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.809T>G MANE Select ENSP00000364336.4:p.Leu270Arg
ENST00000375190.8:c.809T>G ENSP00000364336.3:p.Leu270Arg
ENST00000411851.3:c.809T>G ENSP00000393333.2:p.Leu270Arg
ENST00000589966.1:c.420T>G ENSP00000468145.1:p.Ala140=
NM_001060.5:c.809T>G , LRG_578t1:c.809T>G NP_001051.1:p.Leu270Arg
NM_201636.2:c.809T>G NP_963998.2:p.Leu270Arg
XM_011528214.1:c.809T>G XP_011526516.1:p.Leu270Arg
XM_011528214.2:c.809T>G XP_011526516.1:p.Leu270Arg
NM_001060.6:c.809T>G MANE Select NP_001051.1:p.Leu270Arg
NM_201636.3:c.809T>G NP_963998.2:p.Leu270Arg