Canonical Allele Identifier: CA407439388
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2859312
ClinVar RCV Id: RCV003747822
dbSNP Id: rs1599907495
MyVariant Identifiers: chr19:g.55663207T>C (hg19) chr19:g.55151839T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151839T>C , CM000681.2:g.55151839T>C GRCh38
NC_000019.9:g.55663207T>C , CM000681.1:g.55663207T>C GRCh37
NC_000019.8:g.60355019T>C NCBI36
NG_007866.2:g.10894A>G , LRG_432:g.10894A>G
NG_011829.2:g.2400A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.628A>G MANE Select ENSP00000341838.5:p.Ser210Gly
ENST00000665070.1:c.661A>G ENSP00000499482.1:p.Ser221Gly
ENST00000344887.9:c.628A>G ENSP00000341838.5:p.Ser210Gly
ENST00000585806.5:n.627A>G
ENST00000588882.1:c.553A>G ENSP00000466729.1:p.Ser185Gly
ENST00000589864.1:n.456A>G
NM_000363.4:c.628A>G , LRG_432t1:c.628A>G NP_000354.4:p.Ser210Gly
NM_000363.5:c.628A>G MANE Select NP_000354.4:p.Ser210Gly
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