Canonical Allele Identifier: CA304367826

Gene: TBXA2R

Linked Data

• dbSNP Id: rs200203767
• MyVariant Identifiers: chr19:g.3595596C>G (hg19) ; chr19:g.3595598C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595598C>G , CM000681.2:g.3595598C>G	GRCh38
NC_000019.9:g.3595596C>G , CM000681.1:g.3595596C>G	GRCh37
NC_000019.8:g.3546596C>G	NCBI36
NG_013363.1:g.16236G>C , LRG_578:g.16236G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*90G>C MANE Select	ENSP00000364336.4:n.*90G>C
ENST00000375190.8:c.*90G>C	ENSP00000364336.3:n.*90G>C
ENST00000411851.3:c.983+139G>C	ENSP00000393333.2:n.983+139G>C
ENST00000589966.1:c.733G>C	ENSP00000468145.1:p.Gly245Arg
NM_001060.5:c.*90G>C , LRG_578t1:c.*90G>C	NP_001051.1:n.*90G>C
NM_201636.2:c.983+139G>C	NP_963998.2:n.983+139G>C
XM_011528214.1:c.*90G>C	XP_011526516.1:n.*90G>C
XM_011528214.2:c.*90G>C	XP_011526516.1:n.*90G>C
NM_001060.6:c.*90G>C MANE Select	NP_001051.1:n.*90G>C
NM_201636.3:c.983+139G>C	NP_963998.2:n.983+139G>C