Canonical Allele Identifier: CA304367802

Gene: TBXA2R

Linked Data

• dbSNP Id: rs200202562
• gnomAD v2: 19-3595532-C-G
• gnomAD v3: 19-3595534-C-G
• gnomAD v4: 19-3595534-C-G
• MyVariant Identifiers: chr19:g.3595532C>G (hg19) ; chr19:g.3595534C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595534C>G , CM000681.2:g.3595534C>G	GRCh38
NC_000019.9:g.3595532C>G , CM000681.1:g.3595532C>G	GRCh37
NC_000019.8:g.3546532C>G	NCBI36
NG_013363.1:g.16300G>C , LRG_578:g.16300G>C
NG_031943.1:g.14964C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*154G>C MANE Select	ENSP00000364336.4:n.*154G>C
ENST00000375190.8:c.*154G>C	ENSP00000364336.3:n.*154G>C
ENST00000411851.3:c.983+203G>C	ENSP00000393333.2:n.983+203G>C
ENST00000589966.1:c.*17G>C	ENSP00000468145.1:n.*17G>C
NM_001060.5:c.*154G>C , LRG_578t1:c.*154G>C	NP_001051.1:n.*154G>C
NM_201636.2:c.983+203G>C	NP_963998.2:n.983+203G>C
NM_001060.6:c.*154G>C MANE Select	NP_001051.1:n.*154G>C
NM_201636.3:c.983+203G>C	NP_963998.2:n.983+203G>C