Canonical Allele Identifier: CA508989356
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55663271C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151903C>G , CM000681.2:g.55151903C>G GRCh38
NC_000019.9:g.55663271C>G , CM000681.1:g.55663271C>G GRCh37
NC_000019.8:g.60355083C>G NCBI36
NG_007866.2:g.10830G>C , LRG_432:g.10830G>C
NG_011829.2:g.2336G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.564G>C MANE Select ENSP00000341838.5:p.Val188=
ENST00000665070.1:c.597G>C ENSP00000499482.1:p.Val199=
ENST00000344887.9:c.564G>C ENSP00000341838.5:p.Val188=
ENST00000585806.5:n.563G>C
ENST00000588882.1:c.489G>C ENSP00000466729.1:p.Val163=
ENST00000589864.1:n.392G>C
NM_000363.4:c.564G>C , LRG_432t1:c.564G>C NP_000354.4:p.Val188=
NM_000363.5:c.564G>C MANE Select NP_000354.4:p.Val188=
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