Canonical Allele Identifier: CA379106959
Gene: TNNI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1841527G>C , CM000673.2:g.1841527G>C GRCh38
NC_000011.9:g.1862757G>C , CM000673.1:g.1862757G>C GRCh37
NC_000011.8:g.1819333G>C NCBI36
NG_011621.1:g.7525G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381911.6:c.525G>C MANE Select ENSP00000371336.1:p.Lys175Asn
ENST00000252898.11:c.525G>C ENSP00000252898.7:p.Lys175Asn
ENST00000381905.3:c.525G>C ENSP00000371330.3:p.Lys175Asn
ENST00000381906.5:c.525G>C ENSP00000371331.1:p.Lys175Asn
ENST00000381911.5:c.525G>C ENSP00000371336.1:p.Lys175Asn
ENST00000617947.4:c.525G>C ENSP00000481242.1:p.Lys175Asn
NM_001145829.1:c.525G>C NP_001139301.1:p.Lys175Asn
NM_001145841.1:c.525G>C NP_001139313.1:p.Lys175Asn
NM_003282.3:c.525G>C NP_003273.1:p.Lys175Asn
NM_003282.4:c.525G>C MANE Select NP_003273.1:p.Lys175Asn
NM_001145829.2:c.525G>C NP_001139301.1:p.Lys175Asn
NM_001145841.2:c.525G>C NP_001139313.1:p.Lys175Asn