Canonical Allele Identifier: CA051030

Gene: TNNI3

Linked Data

• dbSNP Id: rs754732148
• ExAC: 19:55667535 G / T
• gnomAD v2: 19-55667535-G-T
• gnomAD v3: 19-55156167-G-T
• gnomAD v4: 19-55156167-G-T
• MyVariant Identifiers: chr19:g.55667535G>T (hg19) ; chr19:g.55156167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156167G>T , CM000681.2:g.55156167G>T	GRCh38
NC_000019.9:g.55667535G>T , CM000681.1:g.55667535G>T	GRCh37
NC_000019.8:g.60359347G>T	NCBI36
NG_007866.2:g.6566C>A , LRG_432:g.6566C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.282+34C>A MANE Select	ENSP00000341838.5:n.282+34C>A
ENST00000665070.1:c.282+34C>A	ENSP00000499482.1:n.282+34C>A
ENST00000344887.9:c.282+34C>A	ENSP00000341838.5:n.282+34C>A
ENST00000585806.5:n.281+34C>A
ENST00000586669.5:n.290+34C>A
ENST00000587176.5:n.466+34C>A
ENST00000587871.1:c.901+34C>A
ENST00000588882.1:c.207+34C>A	ENSP00000466729.1:n.207+34C>A
ENST00000590463.1:n.454+34C>A
NM_000363.4:c.282+34C>A , LRG_432t1:c.282+34C>A	NP_000354.4:n.282+34C>A
NM_000363.5:c.282+34C>A MANE Select	NP_000354.4:n.282+34C>A