Canonical Allele Identifier: CA386869420
Gene: TBX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.115112489G>C (hg19) chr12:g.114674684G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674684G>C , CM000674.2:g.114674684G>C GRCh38
NC_000012.11:g.115112489G>C , CM000674.1:g.115112489G>C GRCh37
NC_000012.10:g.113596872G>C NCBI36
NG_008315.1:g.14481C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000349155.7:c.1191C>G MANE Select ENSP00000257567.2:p.Phe397Leu
ENST00000257566.7:c.1251C>G ENSP00000257566.3:p.Phe417Leu
ENST00000349155.6:c.1191C>G ENSP00000257567.2:p.Phe397Leu
ENST00000613550.1:c.1191C>G ENSP00000480048.1:p.Phe397Leu
NM_005996.3:c.1191C>G NP_005987.3:p.Phe397Leu
NM_016569.3:c.1251C>G NP_057653.3:p.Phe417Leu
NM_005996.4:c.1191C>G MANE Select NP_005987.3:p.Phe397Leu
NM_016569.4:c.1251C>G NP_057653.3:p.Phe417Leu
Search 100 bp 5'
Search 100 bp 3'