Canonical Allele Identifier: CA2318945654
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs2032579289

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595443G>C , CM000681.2:g.3595443G>C GRCh38
NC_000019.9:g.3595441G>C , CM000681.1:g.3595441G>C GRCh37
NC_000019.8:g.3546441G>C NCBI36
NG_013363.1:g.16391C>G , LRG_578:g.16391C>G
NG_031943.1:g.14873G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*245C>G MANE Select ENSP00000364336.4:n.*245C>G
ENST00000375190.8:c.*245C>G ENSP00000364336.3:n.*245C>G
ENST00000411851.3:c.983+294C>G ENSP00000393333.2:n.983+294C>G
ENST00000589966.1:c.*108C>G ENSP00000468145.1:n.*108C>G
NM_001060.5:c.*245C>G , LRG_578t1:c.*245C>G NP_001051.1:n.*245C>G
NM_201636.2:c.983+294C>G NP_963998.2:n.983+294C>G
NM_001060.6:c.*245C>G MANE Select NP_001051.1:n.*245C>G
NM_201636.3:c.983+294C>G NP_963998.2:n.983+294C>G