Canonical Allele Identifier: CA386869720
Gene: TBX3 HGNC NCBI

Linked Data

dbSNP Id: rs899268368
gnomAD v2: 12-115112627-G-T
gnomAD v3: 12-114674822-G-T
gnomAD v4: 12-114674822-G-T
MyVariant Identifiers: chr12:g.115112627G>T (hg19) chr12:g.114674822G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674822G>T , CM000674.2:g.114674822G>T GRCh38
NC_000012.11:g.115112627G>T , CM000674.1:g.115112627G>T GRCh37
NC_000012.10:g.113597010G>T NCBI36
NG_008315.1:g.14343C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1053C>A MANE Select ENSP00000257567.2:p.Ser351Arg
ENST00000257566.7:c.1113C>A ENSP00000257566.3:p.Ser371Arg
ENST00000349155.6:c.1053C>A ENSP00000257567.2:p.Ser351Arg
ENST00000613550.1:c.1053C>A ENSP00000480048.1:p.Ser351Arg
NM_005996.3:c.1053C>A NP_005987.3:p.Ser351Arg
NM_016569.3:c.1113C>A NP_057653.3:p.Ser371Arg
NM_005996.4:c.1053C>A MANE Select NP_005987.3:p.Ser351Arg
NM_016569.4:c.1113C>A NP_057653.3:p.Ser371Arg
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