Canonical Allele Identifier: CA304367746

Gene: TBXA2R

Linked Data

• dbSNP Id: rs964114717
• gnomAD v2: 19-3595355-G-C
• gnomAD v3: 19-3595357-G-C
• gnomAD v4: 19-3595357-G-C
• MyVariant Identifiers: chr19:g.3595355G>C (hg19) ; chr19:g.3595357G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3595357G>C , CM000681.2:g.3595357G>C	GRCh38
NC_000019.9:g.3595355G>C , CM000681.1:g.3595355G>C	GRCh37
NC_000019.8:g.3546355G>C	NCBI36
NG_013363.1:g.16477C>G , LRG_578:g.16477C>G
NG_031943.1:g.14787G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375190.10:c.*331C>G MANE Select	ENSP00000364336.4:n.*331C>G
ENST00000375190.8:c.*331C>G	ENSP00000364336.3:n.*331C>G
ENST00000411851.3:c.984-281C>G	ENSP00000393333.2:n.984-281C>G
ENST00000589966.1:c.*194C>G	ENSP00000468145.1:n.*194C>G
NM_001060.5:c.*331C>G , LRG_578t1:c.*331C>G	NP_001051.1:n.*331C>G
NM_201636.2:c.984-281C>G	NP_963998.2:n.984-281C>G
NM_001060.6:c.*331C>G MANE Select	NP_001051.1:n.*331C>G
NM_201636.3:c.984-281C>G	NP_963998.2:n.984-281C>G