Canonical Allele Identifier: CA022037

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 177863
• ClinVar RCV Id: RCV000154501
• dbSNP Id: rs727504365
• MyVariant Identifiers: chr19:g.55663233A>G (hg19) ; chr19:g.55151865A>G (hg38)
• PubMed: PMID:21533915

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151865A>G , CM000681.2:g.55151865A>G	GRCh38
NC_000019.9:g.55663233A>G , CM000681.1:g.55663233A>G	GRCh37
NC_000019.8:g.60355045A>G	NCBI36
NG_007866.2:g.10868T>C , LRG_432:g.10868T>C
NG_011829.2:g.2374T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.602T>C MANE Select	ENSP00000341838.5:p.Met201Thr
ENST00000665070.1:c.635T>C	ENSP00000499482.1:p.Met212Thr
ENST00000344887.9:c.602T>C	ENSP00000341838.5:p.Met201Thr
ENST00000585806.5:n.601T>C
ENST00000588882.1:c.527T>C	ENSP00000466729.1:p.Met176Thr
ENST00000589864.1:n.430T>C
NM_000363.4:c.602T>C , LRG_432t1:c.602T>C	NP_000354.4:p.Met201Thr
NM_000363.5:c.602T>C MANE Select	NP_000354.4:p.Met201Thr