Canonical Allele Identifier: CA2343273967

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085714873

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154531C>G , CM000681.2:g.55154531C>G	GRCh38
NC_000019.9:g.55665899C>G , CM000681.1:g.55665899C>G	GRCh37
NC_000019.8:g.60357711C>G	NCBI36
NG_007866.2:g.8202G>C , LRG_432:g.8202G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.372+210G>C MANE Select	ENSP00000341838.5:n.372+210G>C
ENST00000665070.1:c.405+177G>C	ENSP00000499482.1:n.405+177G>C
ENST00000344887.9:c.372+210G>C	ENSP00000341838.5:n.372+210G>C
ENST00000585806.5:n.371+210G>C
ENST00000586669.5:n.380+210G>C
ENST00000587176.5:n.766G>C
ENST00000588882.1:c.297+210G>C	ENSP00000466729.1:n.297+210G>C
NM_000363.4:c.372+210G>C , LRG_432t1:c.372+210G>C	NP_000354.4:n.372+210G>C
NM_000363.5:c.372+210G>C MANE Select	NP_000354.4:n.372+210G>C