Canonical Allele Identifier: CA407439709

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55151919-T-G
• MyVariant Identifiers: chr19:g.55663287T>G (hg19) ; chr19:g.55151919T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151919T>G , CM000681.2:g.55151919T>G	GRCh38
NC_000019.9:g.55663287T>G , CM000681.1:g.55663287T>G	GRCh37
NC_000019.8:g.60355099T>G	NCBI36
NG_007866.2:g.10814A>C , LRG_432:g.10814A>C
NG_011829.2:g.2320A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.550-2A>C MANE Select	ENSP00000341838.5:n.550-2A>C
ENST00000665070.1:c.583-2A>C	ENSP00000499482.1:n.583-2A>C
ENST00000344887.9:c.550-2A>C	ENSP00000341838.5:n.550-2A>C
ENST00000585806.5:n.549-2A>C
ENST00000588882.1:c.475-2A>C	ENSP00000466729.1:n.475-2A>C
ENST00000589864.1:n.378-2A>C
NM_000363.4:c.550-2A>C , LRG_432t1:c.550-2A>C	NP_000354.4:n.550-2A>C
NM_000363.5:c.550-2A>C MANE Select	NP_000354.4:n.550-2A>C