Canonical Allele Identifier: CA1947878660
Gene: TNNI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1841468C= , CM000673.2:g.1841468C= GRCh38
NC_000011.9:g.1862698C= , CM000673.1:g.1862698C= GRCh37
NC_000011.8:g.1819274C= NCBI36
NG_011621.1:g.7466C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381911.6:c.466C= MANE Select ENSP00000371336.1:p.Arg156=
ENST00000252898.11:c.466C= ENSP00000252898.7:p.Arg156=
ENST00000381905.3:c.466C= ENSP00000371330.3:p.Arg156=
ENST00000381906.5:c.466C= ENSP00000371331.1:p.Arg156=
ENST00000381911.5:c.466C= ENSP00000371336.1:p.Arg156=
ENST00000617947.4:c.466C= ENSP00000481242.1:p.Arg156=
NM_001145829.1:c.466C= NP_001139301.1:p.Arg156=
NM_001145841.1:c.466C= NP_001139313.1:p.Arg156=
NM_003282.3:c.466C= NP_003273.1:p.Arg156=
NM_003282.4:c.466C= MANE Select NP_003273.1:p.Arg156=
NM_001145829.2:c.466C= NP_001139301.1:p.Arg156=
NM_001145841.2:c.466C= NP_001139313.1:p.Arg156=