Canonical Allele Identifier: CA2318945779

Gene: TBXA2R

Linked Data

• dbSNP Id: rs771062632

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595683A>G , CM000681.2:g.3595683A>G	GRCh38
NC_000019.9:g.3595681A>G , CM000681.1:g.3595681A>G	GRCh37
NC_000019.8:g.3546681A>G	NCBI36
NG_013363.1:g.16151T>C , LRG_578:g.16151T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*5T>C MANE Select	ENSP00000364336.4:n.*5T>C
ENST00000375190.8:c.*5T>C	ENSP00000364336.3:n.*5T>C
ENST00000411851.3:c.983+54T>C	ENSP00000393333.2:n.983+54T>C
ENST00000589966.1:c.648T>C	ENSP00000468145.1:p.Ser216=
NM_001060.5:c.*5T>C , LRG_578t1:c.*5T>C	NP_001051.1:n.*5T>C
NM_201636.2:c.983+54T>C	NP_963998.2:n.983+54T>C
XM_011528214.1:c.*5T>C	XP_011526516.1:n.*5T>C
XM_011528214.2:c.*5T>C	XP_011526516.1:n.*5T>C
NM_001060.6:c.*5T>C MANE Select	NP_001051.1:n.*5T>C
NM_201636.3:c.983+54T>C	NP_963998.2:n.983+54T>C