Canonical Allele Identifier: CA508989528

Gene: TNNI3

Linked Data

• dbSNP Id: rs1599909731
• gnomAD v4: 19-55154827-A-G
• MyVariant Identifiers: chr19:g.55666195A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154827A>G , CM000681.2:g.55154827A>G	GRCh38
NC_000019.9:g.55666195A>G , CM000681.1:g.55666195A>G	GRCh37
NC_000019.8:g.60358007A>G	NCBI36
NG_007866.2:g.7906T>C , LRG_432:g.7906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.286T>C MANE Select	ENSP00000341838.5:p.Leu96=
ENST00000665070.1:c.286T>C	ENSP00000499482.1:p.Leu96=
ENST00000344887.9:c.286T>C	ENSP00000341838.5:p.Leu96=
ENST00000585806.5:n.285T>C
ENST00000586669.5:n.294T>C
ENST00000587176.5:n.470T>C
ENST00000587871.1:c.905T>C
ENST00000588882.1:c.211T>C	ENSP00000466729.1:p.Leu71=
ENST00000590463.1:n.458T>C
NM_000363.4:c.286T>C , LRG_432t1:c.286T>C	NP_000354.4:p.Leu96=
NM_000363.5:c.286T>C MANE Select	NP_000354.4:p.Leu96=