Canonical Allele Identifier: CA051058

Gene: TNNI3

Linked Data

• dbSNP Id: rs766167414
• ExAC: 19:55667520 T / C
• gnomAD v2: 19-55667520-T-C
• gnomAD v4: 19-55156152-T-C
• MyVariant Identifiers: chr19:g.55667520T>C (hg19) ; chr19:g.55156152T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156152T>C , CM000681.2:g.55156152T>C	GRCh38
NC_000019.9:g.55667520T>C , CM000681.1:g.55667520T>C	GRCh37
NC_000019.8:g.60359332T>C	NCBI36
NG_007866.2:g.6581A>G , LRG_432:g.6581A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.282+49A>G MANE Select	ENSP00000341838.5:n.282+49A>G
ENST00000665070.1:c.282+49A>G	ENSP00000499482.1:n.282+49A>G
ENST00000344887.9:c.282+49A>G	ENSP00000341838.5:n.282+49A>G
ENST00000585806.5:n.281+49A>G
ENST00000586669.5:n.290+49A>G
ENST00000587176.5:n.466+49A>G
ENST00000587871.1:c.901+49A>G
ENST00000588882.1:c.207+49A>G	ENSP00000466729.1:n.207+49A>G
ENST00000590463.1:n.454+49A>G
NM_000363.4:c.282+49A>G , LRG_432t1:c.282+49A>G	NP_000354.4:n.282+49A>G
NM_000363.5:c.282+49A>G MANE Select	NP_000354.4:n.282+49A>G