Canonical Allele Identifier: CA2576892652
Gene: TNNI3 HGNC NCBI

Linked Data

gnomAD v4: 19-55154664-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154664G>T , CM000681.2:g.55154664G>T GRCh38
NC_000019.9:g.55666032G>T , CM000681.1:g.55666032G>T GRCh37
NC_000019.8:g.60357844G>T NCBI36
NG_007866.2:g.8069C>A , LRG_432:g.8069C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.372+77C>A MANE Select ENSP00000341838.5:n.372+77C>A
ENST00000665070.1:c.405+44C>A ENSP00000499482.1:n.405+44C>A
ENST00000344887.9:c.372+77C>A ENSP00000341838.5:n.372+77C>A
ENST00000585806.5:n.371+77C>A
ENST00000586669.5:n.380+77C>A
ENST00000587176.5:n.633C>A
ENST00000588882.1:c.297+77C>A ENSP00000466729.1:n.297+77C>A
NM_000363.4:c.372+77C>A , LRG_432t1:c.372+77C>A NP_000354.4:n.372+77C>A
NM_000363.5:c.372+77C>A MANE Select NP_000354.4:n.372+77C>A
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