Canonical Allele Identifier: CA508989380
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665434G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154066G>C , CM000681.2:g.55154066G>C GRCh38
NC_000019.9:g.55665434G>C , CM000681.1:g.55665434G>C GRCh37
NC_000019.8:g.60357246G>C NCBI36
NG_007866.2:g.8667C>G , LRG_432:g.8667C>G
NG_011829.2:g.173C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.513C>G MANE Select ENSP00000341838.5:p.Ala171=
ENST00000665070.1:c.546C>G ENSP00000499482.1:p.Ala182=
ENST00000344887.9:c.513C>G ENSP00000341838.5:p.Ala171=
ENST00000585806.5:n.512C>G
ENST00000588882.1:c.438C>G ENSP00000466729.1:p.Ala146=
ENST00000589864.1:n.341C>G
NM_000363.4:c.513C>G , LRG_432t1:c.513C>G NP_000354.4:p.Ala171=
NM_000363.5:c.513C>G MANE Select NP_000354.4:p.Ala171=
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