Canonical Allele Identifier: CA883724501

Gene: TNNI3

Linked Data

• dbSNP Id: rs932998138
• gnomAD v4: 19-55156125-C-T
• MyVariant Identifiers: chr19:g.55667493C>T (hg19) ; chr19:g.55156125C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156125C>T , CM000681.2:g.55156125C>T	GRCh38
NC_000019.9:g.55667493C>T , CM000681.1:g.55667493C>T	GRCh37
NC_000019.8:g.60359305C>T	NCBI36
NG_007866.2:g.6608G>A , LRG_432:g.6608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.282+76G>A MANE Select	ENSP00000341838.5:n.282+76G>A
ENST00000665070.1:c.282+76G>A	ENSP00000499482.1:n.282+76G>A
ENST00000344887.9:c.282+76G>A	ENSP00000341838.5:n.282+76G>A
ENST00000585806.5:n.281+76G>A
ENST00000586669.5:n.290+76G>A
ENST00000587176.5:n.466+76G>A
ENST00000587871.1:c.901+76G>A
ENST00000588882.1:c.207+76G>A	ENSP00000466729.1:n.207+76G>A
ENST00000590463.1:n.454+76G>A
NM_000363.4:c.282+76G>A , LRG_432t1:c.282+76G>A	NP_000354.4:n.282+76G>A
NM_000363.5:c.282+76G>A MANE Select	NP_000354.4:n.282+76G>A