Canonical Allele Identifier: CA051723

Gene: TNNI3

Linked Data

• dbSNP Id: rs766278642
• ExAC: 19:55665369 C / G
• gnomAD v2: 19-55665369-C-G
• gnomAD v4: 19-55154001-C-G
• MyVariant Identifiers: chr19:g.55665369C>G (hg19) ; chr19:g.55154001C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154001C>G , CM000681.2:g.55154001C>G	GRCh38
NC_000019.9:g.55665369C>G , CM000681.1:g.55665369C>G	GRCh37
NC_000019.8:g.60357181C>G	NCBI36
NG_007866.2:g.8732G>C , LRG_432:g.8732G>C
NG_011829.2:g.238G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.549+29G>C MANE Select	ENSP00000341838.5:n.549+29G>C
ENST00000665070.1:c.582+29G>C	ENSP00000499482.1:n.582+29G>C
ENST00000344887.9:c.549+29G>C	ENSP00000341838.5:n.549+29G>C
ENST00000585806.5:n.548+29G>C
ENST00000588882.1:c.474+29G>C	ENSP00000466729.1:n.474+29G>C
ENST00000589864.1:n.377+29G>C
NM_000363.4:c.549+29G>C , LRG_432t1:c.549+29G>C	NP_000354.4:n.549+29G>C
NM_000363.5:c.549+29G>C MANE Select	NP_000354.4:n.549+29G>C