Canonical Allele Identifier: CA883721822

Gene: TNNI3

Linked Data

• dbSNP Id: rs1273647767
• gnomAD v3: 19-55153804-A-C
• gnomAD v4: 19-55153804-A-C
• MyVariant Identifiers: chr19:g.55665172A>C (hg19) ; chr19:g.55153804A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153804A>C , CM000681.2:g.55153804A>C	GRCh38
NC_000019.9:g.55665172A>C , CM000681.1:g.55665172A>C	GRCh37
NC_000019.8:g.60356984A>C	NCBI36
NG_007866.2:g.8929T>G , LRG_432:g.8929T>G
NG_011829.2:g.435T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+226T>G MANE Select	ENSP00000341838.5:n.549+226T>G
ENST00000665070.1:c.582+226T>G	ENSP00000499482.1:n.582+226T>G
ENST00000344887.9:c.549+226T>G	ENSP00000341838.5:n.549+226T>G
ENST00000585806.5:n.548+226T>G
ENST00000588882.1:c.474+226T>G	ENSP00000466729.1:n.474+226T>G
ENST00000589864.1:n.377+226T>G
NM_000363.4:c.549+226T>G , LRG_432t1:c.549+226T>G	NP_000354.4:n.549+226T>G
NM_000363.5:c.549+226T>G MANE Select	NP_000354.4:n.549+226T>G