Canonical Allele Identifier: CA407440307
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665442G>C (hg19) chr19:g.55154074G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154074G>C , CM000681.2:g.55154074G>C GRCh38
NC_000019.9:g.55665442G>C , CM000681.1:g.55665442G>C GRCh37
NC_000019.8:g.60357254G>C NCBI36
NG_007866.2:g.8659C>G , LRG_432:g.8659C>G
NG_011829.2:g.165C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.505C>G MANE Select ENSP00000341838.5:p.Leu169Val
ENST00000665070.1:c.538C>G ENSP00000499482.1:p.Leu180Val
ENST00000344887.9:c.505C>G ENSP00000341838.5:p.Leu169Val
ENST00000585806.5:n.504C>G
ENST00000588882.1:c.430C>G ENSP00000466729.1:p.Leu144Val
ENST00000589864.1:n.333C>G
NM_000363.4:c.505C>G , LRG_432t1:c.505C>G NP_000354.4:p.Leu169Val
NM_000363.5:c.505C>G MANE Select NP_000354.4:p.Leu169Val
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