Canonical Allele Identifier: CA508989377
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665428G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154060G>C , CM000681.2:g.55154060G>C GRCh38
NC_000019.9:g.55665428G>C , CM000681.1:g.55665428G>C GRCh37
NC_000019.8:g.60357240G>C NCBI36
NG_007866.2:g.8673C>G , LRG_432:g.8673C>G
NG_011829.2:g.179C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.519C>G MANE Select ENSP00000341838.5:p.Leu173=
ENST00000665070.1:c.552C>G ENSP00000499482.1:p.Leu184=
ENST00000344887.9:c.519C>G ENSP00000341838.5:p.Leu173=
ENST00000585806.5:n.518C>G
ENST00000588882.1:c.444C>G ENSP00000466729.1:p.Leu148=
ENST00000589864.1:n.347C>G
NM_000363.4:c.519C>G , LRG_432t1:c.519C>G NP_000354.4:p.Leu173=
NM_000363.5:c.519C>G MANE Select NP_000354.4:p.Leu173=
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