Canonical Allele Identifier: CA883722871

Gene: TNNI3

Linked Data

• dbSNP Id: rs1176139941
• gnomAD v4: 19-55154636-C-T
• MyVariant Identifiers: chr19:g.55666004C>T (hg19) ; chr19:g.55154636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154636C>T , CM000681.2:g.55154636C>T	GRCh38
NC_000019.9:g.55666004C>T , CM000681.1:g.55666004C>T	GRCh37
NC_000019.8:g.60357816C>T	NCBI36
NG_007866.2:g.8097G>A , LRG_432:g.8097G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.372+105G>A MANE Select	ENSP00000341838.5:n.372+105G>A
ENST00000665070.1:c.405+72G>A	ENSP00000499482.1:n.405+72G>A
ENST00000344887.9:c.372+105G>A	ENSP00000341838.5:n.372+105G>A
ENST00000585806.5:n.371+105G>A
ENST00000586669.5:n.380+105G>A
ENST00000587176.5:n.661G>A
ENST00000588882.1:c.297+105G>A	ENSP00000466729.1:n.297+105G>A
NM_000363.4:c.372+105G>A , LRG_432t1:c.372+105G>A	NP_000354.4:n.372+105G>A
NM_000363.5:c.372+105G>A MANE Select	NP_000354.4:n.372+105G>A