Canonical Allele Identifier: CA304367744

Gene: TBXA2R

Linked Data

• dbSNP Id: rs200453213
• gnomAD v2: 19-3595349-C-G
• gnomAD v3: 19-3595351-C-G
• gnomAD v4: 19-3595351-C-G
• MyVariant Identifiers: chr19:g.3595349C>G (hg19) ; chr19:g.3595351C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595351C>G , CM000681.2:g.3595351C>G	GRCh38
NC_000019.9:g.3595349C>G , CM000681.1:g.3595349C>G	GRCh37
NC_000019.8:g.3546349C>G	NCBI36
NG_013363.1:g.16483G>C , LRG_578:g.16483G>C
NG_031943.1:g.14781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*337G>C MANE Select	ENSP00000364336.4:n.*337G>C
ENST00000375190.8:c.*337G>C	ENSP00000364336.3:n.*337G>C
ENST00000411851.3:c.984-275G>C	ENSP00000393333.2:n.984-275G>C
ENST00000589966.1:c.*200G>C	ENSP00000468145.1:n.*200G>C
NM_001060.5:c.*337G>C , LRG_578t1:c.*337G>C	NP_001051.1:n.*337G>C
NM_201636.2:c.984-275G>C	NP_963998.2:n.984-275G>C
NM_001060.6:c.*337G>C MANE Select	NP_001051.1:n.*337G>C
NM_201636.3:c.984-275G>C	NP_963998.2:n.984-275G>C