Canonical Allele Identifier: CA633870712

Gene: TNNI3

Linked Data

• dbSNP Id: rs1380580911
• gnomAD v2: 19-55665100-A-C
• gnomAD v3: 19-55153732-A-C
• gnomAD v4: 19-55153732-A-C
• MyVariant Identifiers: chr19:g.55665100A>C (hg19) ; chr19:g.55153732A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153732A>C , CM000681.2:g.55153732A>C	GRCh38
NC_000019.9:g.55665100A>C , CM000681.1:g.55665100A>C	GRCh37
NC_000019.8:g.60356912A>C	NCBI36
NG_007866.2:g.9001T>G , LRG_432:g.9001T>G
NG_011829.2:g.507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+298T>G MANE Select	ENSP00000341838.5:n.549+298T>G
ENST00000665070.1:c.582+298T>G	ENSP00000499482.1:n.582+298T>G
ENST00000344887.9:c.549+298T>G	ENSP00000341838.5:n.549+298T>G
ENST00000585806.5:n.548+298T>G
ENST00000588882.1:c.474+298T>G	ENSP00000466729.1:n.474+298T>G
ENST00000589864.1:n.377+298T>G
NM_000363.4:c.549+298T>G , LRG_432t1:c.549+298T>G	NP_000354.4:n.549+298T>G
NM_000363.5:c.549+298T>G MANE Select	NP_000354.4:n.549+298T>G