Canonical Allele Identifier: CA310149687

Gene: TNNI3

Linked Data

• dbSNP Id: rs1005194590
• gnomAD v2: 19-55667539-T-G
• gnomAD v3: 19-55156171-T-G
• gnomAD v4: 19-55156171-T-G
• MyVariant Identifiers: chr19:g.55667539T>G (hg19) ; chr19:g.55156171T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156171T>G , CM000681.2:g.55156171T>G	GRCh38
NC_000019.9:g.55667539T>G , CM000681.1:g.55667539T>G	GRCh37
NC_000019.8:g.60359351T>G	NCBI36
NG_007866.2:g.6562A>C , LRG_432:g.6562A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.282+30A>C MANE Select	ENSP00000341838.5:n.282+30A>C
ENST00000665070.1:c.282+30A>C	ENSP00000499482.1:n.282+30A>C
ENST00000344887.9:c.282+30A>C	ENSP00000341838.5:n.282+30A>C
ENST00000585806.5:n.281+30A>C
ENST00000586669.5:n.290+30A>C
ENST00000587176.5:n.466+30A>C
ENST00000587871.1:c.901+30A>C
ENST00000588882.1:c.207+30A>C	ENSP00000466729.1:n.207+30A>C
ENST00000590463.1:n.454+30A>C
NM_000363.4:c.282+30A>C , LRG_432t1:c.282+30A>C	NP_000354.4:n.282+30A>C
NM_000363.5:c.282+30A>C MANE Select	NP_000354.4:n.282+30A>C