Canonical Allele Identifier: CA883720665

Gene: TNNI3

Linked Data

• dbSNP Id: rs1231688200
• gnomAD v3: 19-55152154-T-C
• gnomAD v4: 19-55152154-T-C
• MyVariant Identifiers: chr19:g.55663522T>C (hg19) ; chr19:g.55152154T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152154T>C , CM000681.2:g.55152154T>C	GRCh38
NC_000019.9:g.55663522T>C , CM000681.1:g.55663522T>C	GRCh37
NC_000019.8:g.60355334T>C	NCBI36
NG_007866.2:g.10579A>G , LRG_432:g.10579A>G
NG_011829.2:g.2085A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-237A>G MANE Select	ENSP00000341838.5:n.550-237A>G
ENST00000665070.1:c.583-237A>G	ENSP00000499482.1:n.583-237A>G
ENST00000344887.9:c.550-237A>G	ENSP00000341838.5:n.550-237A>G
ENST00000585806.5:n.549-237A>G
ENST00000588882.1:c.475-237A>G	ENSP00000466729.1:n.475-237A>G
ENST00000589864.1:n.378-237A>G
NM_000363.4:c.550-237A>G , LRG_432t1:c.550-237A>G	NP_000354.4:n.550-237A>G
NM_000363.5:c.550-237A>G MANE Select	NP_000354.4:n.550-237A>G