Canonical Allele Identifier: CA508989427
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665494T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154126T>C , CM000681.2:g.55154126T>C GRCh38
NC_000019.9:g.55665494T>C , CM000681.1:g.55665494T>C GRCh37
NC_000019.8:g.60357306T>C NCBI36
NG_007866.2:g.8607A>G , LRG_432:g.8607A>G
NG_011829.2:g.113A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.453A>G MANE Select ENSP00000341838.5:p.Ala151=
ENST00000665070.1:c.486A>G ENSP00000499482.1:p.Ala162=
ENST00000344887.9:c.453A>G ENSP00000341838.5:p.Ala151=
ENST00000585806.5:n.452A>G
ENST00000586669.5:n.461A>G
ENST00000588882.1:c.378A>G ENSP00000466729.1:p.Ala126=
ENST00000589864.1:n.281A>G
NM_000363.4:c.453A>G , LRG_432t1:c.453A>G NP_000354.4:p.Ala151=
NM_000363.5:c.453A>G MANE Select NP_000354.4:p.Ala151=