Canonical Allele Identifier: CA5815094
Gene: TNNI2 HGNC NCBI

Linked Data

dbSNP Id: rs907610
gnomAD v2: 11-1861760-T-A
gnomAD v4: 11-1840530-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840530T>A , CM000673.2:g.1840530T>A GRCh38
NC_000011.9:g.1861760T>A , CM000673.1:g.1861760T>A GRCh37
NC_000011.8:g.1818336T>A NCBI36
NG_011621.1:g.6528T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.60T>A MANE Select ENSP00000371336.1:p.Ser20Arg
ENST00000252898.11:c.60T>A ENSP00000252898.7:p.Ser20Arg
ENST00000381905.3:c.60T>A ENSP00000371330.3:p.Ser20Arg
ENST00000381906.5:c.60T>A ENSP00000371331.1:p.Ser20Arg
ENST00000381911.5:c.60T>A ENSP00000371336.1:p.Ser20Arg
ENST00000468473.1:n.230T>A
ENST00000617947.4:c.60T>A ENSP00000481242.1:p.Ser20Arg
NM_001145829.1:c.60T>A NP_001139301.1:p.Ser20Arg
NM_001145841.1:c.60T>A NP_001139313.1:p.Ser20Arg
NM_003282.3:c.60T>A NP_003273.1:p.Ser20Arg
NM_003282.4:c.60T>A MANE Select NP_003273.1:p.Ser20Arg
NM_001145829.2:c.60T>A NP_001139301.1:p.Ser20Arg
NM_001145841.2:c.60T>A NP_001139313.1:p.Ser20Arg