Canonical Allele Identifier: CA633906536

Gene: TNNI3

Linked Data

• dbSNP Id: rs1308747121
• gnomAD v2: 19-55667524-G-A
• gnomAD v4: 19-55156156-G-A
• MyVariant Identifiers: chr19:g.55667524G>A (hg19) ; chr19:g.55156156G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156156G>A , CM000681.2:g.55156156G>A	GRCh38
NC_000019.9:g.55667524G>A , CM000681.1:g.55667524G>A	GRCh37
NC_000019.8:g.60359336G>A	NCBI36
NG_007866.2:g.6577C>T , LRG_432:g.6577C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.282+45C>T MANE Select	ENSP00000341838.5:n.282+45C>T
ENST00000665070.1:c.282+45C>T	ENSP00000499482.1:n.282+45C>T
ENST00000344887.9:c.282+45C>T	ENSP00000341838.5:n.282+45C>T
ENST00000585806.5:n.281+45C>T
ENST00000586669.5:n.290+45C>T
ENST00000587176.5:n.466+45C>T
ENST00000587871.1:c.901+45C>T
ENST00000588882.1:c.207+45C>T	ENSP00000466729.1:n.207+45C>T
ENST00000590463.1:n.454+45C>T
NM_000363.4:c.282+45C>T , LRG_432t1:c.282+45C>T	NP_000354.4:n.282+45C>T
NM_000363.5:c.282+45C>T MANE Select	NP_000354.4:n.282+45C>T