Canonical Allele Identifier: CA403329054
Gene: TBXA2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.3595574C>G (hg19) chr19:g.3595576C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595576C>G , CM000681.2:g.3595576C>G GRCh38
NC_000019.9:g.3595574C>G , CM000681.1:g.3595574C>G GRCh37
NC_000019.8:g.3546574C>G NCBI36
NG_013363.1:g.16258G>C , LRG_578:g.16258G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*112G>C MANE Select ENSP00000364336.4:n.*112G>C
ENST00000375190.8:c.*112G>C ENSP00000364336.3:n.*112G>C
ENST00000411851.3:c.983+161G>C ENSP00000393333.2:n.983+161G>C
ENST00000589966.1:c.755G>C ENSP00000468145.1:p.Gly252Ala
NM_001060.5:c.*112G>C , LRG_578t1:c.*112G>C NP_001051.1:n.*112G>C
NM_201636.2:c.983+161G>C NP_963998.2:n.983+161G>C
NM_001060.6:c.*112G>C MANE Select NP_001051.1:n.*112G>C
NM_201636.3:c.983+161G>C NP_963998.2:n.983+161G>C
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