Canonical Allele Identifier: CA997261364
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085710544

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153975G>A , CM000681.2:g.55153975G>A GRCh38
NC_000019.9:g.55665343G>A , CM000681.1:g.55665343G>A GRCh37
NC_000019.8:g.60357155G>A NCBI36
NG_007866.2:g.8758C>T , LRG_432:g.8758C>T
NG_011829.2:g.264C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+55C>T MANE Select ENSP00000341838.5:n.549+55C>T
ENST00000665070.1:c.582+55C>T ENSP00000499482.1:n.582+55C>T
ENST00000344887.9:c.549+55C>T ENSP00000341838.5:n.549+55C>T
ENST00000585806.5:n.548+55C>T
ENST00000588882.1:c.474+55C>T ENSP00000466729.1:n.474+55C>T
ENST00000589864.1:n.377+55C>T
NM_000363.4:c.549+55C>T , LRG_432t1:c.549+55C>T NP_000354.4:n.549+55C>T
NM_000363.5:c.549+55C>T MANE Select NP_000354.4:n.549+55C>T