Canonical Allele Identifier: CA051718

Gene: TNNI3

Linked Data

• dbSNP Id: rs776950520
• ExAC: 19:55665378 T / C
• gnomAD v2: 19-55665378-T-C
• gnomAD v4: 19-55154010-T-C
• MyVariant Identifiers: chr19:g.55665378T>C (hg19) ; chr19:g.55154010T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154010T>C , CM000681.2:g.55154010T>C	GRCh38
NC_000019.9:g.55665378T>C , CM000681.1:g.55665378T>C	GRCh37
NC_000019.8:g.60357190T>C	NCBI36
NG_007866.2:g.8723A>G , LRG_432:g.8723A>G
NG_011829.2:g.229A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.549+20A>G MANE Select	ENSP00000341838.5:n.549+20A>G
ENST00000665070.1:c.582+20A>G	ENSP00000499482.1:n.582+20A>G
ENST00000344887.9:c.549+20A>G	ENSP00000341838.5:n.549+20A>G
ENST00000585806.5:n.548+20A>G
ENST00000588882.1:c.474+20A>G	ENSP00000466729.1:n.474+20A>G
ENST00000589864.1:n.377+20A>G
NM_000363.4:c.549+20A>G , LRG_432t1:c.549+20A>G	NP_000354.4:n.549+20A>G
NM_000363.5:c.549+20A>G MANE Select	NP_000354.4:n.549+20A>G