Canonical Allele Identifier: CA471993277

Gene: TNNI2

Linked Data

• MyVariant Identifiers: chr11:g.1862766T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841536T>C , CM000673.2:g.1841536T>C	GRCh38
NC_000011.9:g.1862766T>C , CM000673.1:g.1862766T>C	GRCh37
NC_000011.8:g.1819342T>C	NCBI36
NG_011621.1:g.7534T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.534T>C MANE Select	ENSP00000371336.1:p.Phe178=
ENST00000252898.11:c.534T>C	ENSP00000252898.7:p.Phe178=
ENST00000381905.3:c.534T>C	ENSP00000371330.3:p.Phe178=
ENST00000381906.5:c.534T>C	ENSP00000371331.1:p.Phe178=
ENST00000381911.5:c.534T>C	ENSP00000371336.1:p.Phe178=
ENST00000617947.4:c.534T>C	ENSP00000481242.1:p.Phe178=
NM_001145829.1:c.534T>C	NP_001139301.1:p.Phe178=
NM_001145841.1:c.534T>C	NP_001139313.1:p.Phe178=
NM_003282.3:c.534T>C	NP_003273.1:p.Phe178=
NM_003282.4:c.534T>C MANE Select	NP_003273.1:p.Phe178=
NM_001145829.2:c.534T>C	NP_001139301.1:p.Phe178=
NM_001145841.2:c.534T>C	NP_001139313.1:p.Phe178=