Canonical Allele Identifier: CA407440587

Gene: TNNI3

Linked Data

• ClinVar Variation Id: 920147
• ClinVar RCV Id: RCV001178726 ; RCV002555493 ; RCV002327433
• dbSNP Id: rs730881071
• MyVariant Identifiers: chr19:g.55665526G>C (hg19) ; chr19:g.55154158G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154158G>C , CM000681.2:g.55154158G>C	GRCh38
NC_000019.9:g.55665526G>C , CM000681.1:g.55665526G>C	GRCh37
NC_000019.8:g.60357338G>C	NCBI36
NG_007866.2:g.8575C>G , LRG_432:g.8575C>G
NG_011829.2:g.81C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.421C>G MANE Select	ENSP00000341838.5:p.Arg141Gly
ENST00000665070.1:c.454C>G	ENSP00000499482.1:p.Arg152Gly
ENST00000344887.9:c.421C>G	ENSP00000341838.5:p.Arg141Gly
ENST00000585806.5:n.420C>G
ENST00000586669.5:n.429C>G
ENST00000588882.1:c.346C>G	ENSP00000466729.1:p.Arg116Gly
ENST00000589864.1:n.249C>G
NM_000363.4:c.421C>G , LRG_432t1:c.421C>G	NP_000354.4:p.Arg141Gly
NM_000363.5:c.421C>G MANE Select	NP_000354.4:p.Arg141Gly