Canonical Allele Identifier: CA304367752

Gene: TBXA2R

Linked Data

• dbSNP Id: rs528449012
• MyVariant Identifiers: chr19:g.3595374_3595375insTT (hg19) ; chr19:g.3595376_3595377insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595377_3595378insTT , CM000681.2:g.3595377_3595378insTT	GRCh38
NC_000019.9:g.3595375_3595376insTT , CM000681.1:g.3595375_3595376insTT	GRCh37
NC_000019.8:g.3546375_3546376insTT	NCBI36
NG_013363.1:g.16457_16458insAA , LRG_578:g.16457_16458insAA
NG_031943.1:g.14807_14808insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*311_*312insAA MANE Select	ENSP00000364336.4:n.*311_*312insAA
ENST00000375190.8:c.*311_*312insAA	ENSP00000364336.3:n.*311_*312insAA
ENST00000411851.3:c.984-301_984-300insAA	ENSP00000393333.2:n.984-301_984-300insAA
ENST00000589966.1:c.*174_*175insAA	ENSP00000468145.1:n.*174_*175insAA
NM_001060.5:c.*311_*312insAA , LRG_578t1:c.*311_*312insAA	NP_001051.1:n.*311_*312insAA
NM_201636.2:c.984-301_984-300insAA	NP_963998.2:n.984-301_984-300insAA
NM_001060.6:c.*311_*312insAA MANE Select	NP_001051.1:n.*311_*312insAA
NM_201636.3:c.984-301_984-300insAA	NP_963998.2:n.984-301_984-300insAA