Canonical Allele Identifier: CA051002

Gene: TNNI3

Linked Data

• dbSNP Id: rs777905698
• ExAC: 19:55667546 C / G
• gnomAD v2: 19-55667546-C-G
• gnomAD v3: 19-55156178-C-G
• gnomAD v4: 19-55156178-C-G
• MyVariant Identifiers: chr19:g.55667546C>G (hg19) ; chr19:g.55156178C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156178C>G , CM000681.2:g.55156178C>G	GRCh38
NC_000019.9:g.55667546C>G , CM000681.1:g.55667546C>G	GRCh37
NC_000019.8:g.60359358C>G	NCBI36
NG_007866.2:g.6555G>C , LRG_432:g.6555G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.282+23G>C MANE Select	ENSP00000341838.5:n.282+23G>C
ENST00000665070.1:c.282+23G>C	ENSP00000499482.1:n.282+23G>C
ENST00000344887.9:c.282+23G>C	ENSP00000341838.5:n.282+23G>C
ENST00000585806.5:n.281+23G>C
ENST00000586669.5:n.290+23G>C
ENST00000587176.5:n.466+23G>C
ENST00000587871.1:c.901+23G>C
ENST00000588882.1:c.207+23G>C	ENSP00000466729.1:n.207+23G>C
ENST00000590463.1:n.454+23G>C
NM_000363.4:c.282+23G>C , LRG_432t1:c.282+23G>C	NP_000354.4:n.282+23G>C
NM_000363.5:c.282+23G>C MANE Select	NP_000354.4:n.282+23G>C