Canonical Allele Identifier: CA310144922

Gene: TNNI3

Linked Data

• dbSNP Id: rs796550160
• MyVariant Identifiers: chr19:g.55663263C>T (hg19) ; chr19:g.55151895C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151895C>T , CM000681.2:g.55151895C>T	GRCh38
NC_000019.9:g.55663263C>T , CM000681.1:g.55663263C>T	GRCh37
NC_000019.8:g.60355075C>T	NCBI36
NG_007866.2:g.10838G>A , LRG_432:g.10838G>A
NG_011829.2:g.2344G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.572G>A MANE Select	ENSP00000341838.5:p.Trp191Ter
ENST00000665070.1:c.605G>A	ENSP00000499482.1:p.Trp202Ter
ENST00000344887.9:c.572G>A	ENSP00000341838.5:p.Trp191Ter
ENST00000585806.5:n.571G>A
ENST00000588882.1:c.497G>A	ENSP00000466729.1:p.Trp166Ter
ENST00000589864.1:n.400G>A
NM_000363.4:c.572G>A , LRG_432t1:c.572G>A	NP_000354.4:p.Trp191Ter
NM_000363.5:c.572G>A MANE Select	NP_000354.4:p.Trp191Ter