Canonical Allele Identifier: CA216206447
Gene: TNNI2 HGNC NCBI

Linked Data

dbSNP Id: rs1001708492
gnomAD v4: 11-1841635-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1841635G>C , CM000673.2:g.1841635G>C GRCh38
NC_000011.9:g.1862865G>C , CM000673.1:g.1862865G>C GRCh37
NC_000011.8:g.1819441G>C NCBI36
NG_011621.1:g.7633G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.*84G>C MANE Select ENSP00000371336.1:n.*84G>C
ENST00000252898.11:c.633G>C ENSP00000252898.7:n.633G>C
ENST00000381905.3:c.*84G>C ENSP00000371330.3:n.*84G>C
ENST00000381906.5:c.*84G>C ENSP00000371331.1:n.*84G>C
ENST00000381911.5:c.*84G>C ENSP00000371336.1:n.*84G>C
ENST00000617947.4:c.*84G>C ENSP00000481242.1:n.*84G>C
NM_001145829.1:c.*84G>C NP_001139301.1:n.*84G>C
NM_001145841.1:c.*84G>C NP_001139313.1:n.*84G>C
NM_003282.3:c.*84G>C NP_003273.1:n.*84G>C
NM_003282.4:c.*84G>C MANE Select NP_003273.1:n.*84G>C
NM_001145829.2:c.*84G>C NP_001139301.1:n.*84G>C
NM_001145841.2:c.*84G>C NP_001139313.1:n.*84G>C