Canonical Allele Identifier: CA403329138

Gene: TBXA2R

Linked Data

• MyVariant Identifiers: chr19:g.3595595C>T (hg19) ; chr19:g.3595597C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595597C>T , CM000681.2:g.3595597C>T	GRCh38
NC_000019.9:g.3595595C>T , CM000681.1:g.3595595C>T	GRCh37
NC_000019.8:g.3546595C>T	NCBI36
NG_013363.1:g.16237G>A , LRG_578:g.16237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*91G>A MANE Select	ENSP00000364336.4:n.*91G>A
ENST00000375190.8:c.*91G>A	ENSP00000364336.3:n.*91G>A
ENST00000411851.3:c.983+140G>A	ENSP00000393333.2:n.983+140G>A
ENST00000589966.1:c.734G>A	ENSP00000468145.1:p.Gly245Glu
NM_001060.5:c.*91G>A , LRG_578t1:c.*91G>A	NP_001051.1:n.*91G>A
NM_201636.2:c.983+140G>A	NP_963998.2:n.983+140G>A
XM_011528214.2:c.*91G>A	XP_011526516.1:n.*91G>A
NM_001060.6:c.*91G>A MANE Select	NP_001051.1:n.*91G>A
NM_201636.3:c.983+140G>A	NP_963998.2:n.983+140G>A