Canonical Allele Identifier: CA407440417

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085712011
• MyVariant Identifiers: chr19:g.55665481G>A (hg19) ; chr19:g.55154113G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154113G>A , CM000681.2:g.55154113G>A	GRCh38
NC_000019.9:g.55665481G>A , CM000681.1:g.55665481G>A	GRCh37
NC_000019.8:g.60357293G>A	NCBI36
NG_007866.2:g.8620C>T , LRG_432:g.8620C>T
NG_011829.2:g.126C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.466C>T MANE Select	ENSP00000341838.5:p.Gln156Ter
ENST00000665070.1:c.499C>T	ENSP00000499482.1:p.Gln167Ter
ENST00000344887.9:c.466C>T	ENSP00000341838.5:p.Gln156Ter
ENST00000585806.5:n.465C>T
ENST00000586669.5:n.474C>T
ENST00000588882.1:c.391C>T	ENSP00000466729.1:p.Gln131Ter
ENST00000589864.1:n.294C>T
NM_000363.4:c.466C>T , LRG_432t1:c.466C>T	NP_000354.4:p.Gln156Ter
NM_000363.5:c.466C>T MANE Select	NP_000354.4:p.Gln156Ter