Canonical Allele Identifier: CA508989455
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665526G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154158G>T , CM000681.2:g.55154158G>T GRCh38
NC_000019.9:g.55665526G>T , CM000681.1:g.55665526G>T GRCh37
NC_000019.8:g.60357338G>T NCBI36
NG_007866.2:g.8575C>A , LRG_432:g.8575C>A
NG_011829.2:g.81C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.421C>A MANE Select ENSP00000341838.5:p.Arg141=
ENST00000665070.1:c.454C>A ENSP00000499482.1:p.Arg152=
ENST00000344887.9:c.421C>A ENSP00000341838.5:p.Arg141=
ENST00000585806.5:n.420C>A
ENST00000586669.5:n.429C>A
ENST00000588882.1:c.346C>A ENSP00000466729.1:p.Arg116=
ENST00000589864.1:n.249C>A
NM_000363.4:c.421C>A , LRG_432t1:c.421C>A NP_000354.4:p.Arg141=
NM_000363.5:c.421C>A MANE Select NP_000354.4:p.Arg141=
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