Canonical Allele Identifier: CA407441954

Gene: TNNI3

Linked Data

• dbSNP Id: rs1487255292
• gnomAD v2: 19-55667671-C-A
• MyVariant Identifiers: chr19:g.55667671C>A (hg19) ; chr19:g.55156303C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156303C>A , CM000681.2:g.55156303C>A	GRCh38
NC_000019.9:g.55667671C>A , CM000681.1:g.55667671C>A	GRCh37
NC_000019.8:g.60359483C>A	NCBI36
NG_007866.2:g.6430G>T , LRG_432:g.6430G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.180G>T MANE Select	ENSP00000341838.5:p.Glu60Asp
ENST00000665070.1:c.180G>T	ENSP00000499482.1:p.Glu60Asp
ENST00000344887.9:c.180G>T	ENSP00000341838.5:p.Glu60Asp
ENST00000585806.5:n.179G>T
ENST00000586669.5:n.188G>T
ENST00000586858.1:c.143G>T	ENSP00000465258.1:p.Ser48Ile
ENST00000587176.5:n.364G>T
ENST00000587871.1:c.799G>T
ENST00000588882.1:c.105G>T	ENSP00000466729.1:p.Glu35Asp
ENST00000590463.1:n.352G>T
NM_000363.4:c.180G>T , LRG_432t1:c.180G>T	NP_000354.4:p.Glu60Asp
NM_000363.5:c.180G>T MANE Select	NP_000354.4:p.Glu60Asp