Canonical Allele Identifier: CA472106139
Gene: TNNI2 HGNC NCBI

Linked Data

dbSNP Id: rs1462064702
gnomAD v2: 11-1861805-C-T
gnomAD v3: 11-1840575-C-T
gnomAD v4: 11-1840575-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840575C>T , CM000673.2:g.1840575C>T GRCh38
NC_000011.9:g.1861805C>T , CM000673.1:g.1861805C>T GRCh37
NC_000011.8:g.1818381C>T NCBI36
NG_011621.1:g.6573C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.105C>T MANE Select ENSP00000371336.1:p.Ser35=
ENST00000252898.11:c.105C>T ENSP00000252898.7:p.Ser35=
ENST00000381905.3:c.105C>T ENSP00000371330.3:p.Ser35=
ENST00000381906.5:c.105C>T ENSP00000371331.1:p.Ser35=
ENST00000381911.5:c.105C>T ENSP00000371336.1:p.Ser35=
ENST00000468473.1:n.275C>T
ENST00000617947.4:c.105C>T ENSP00000481242.1:p.Ser35=
NM_001145829.1:c.105C>T NP_001139301.1:p.Ser35=
NM_001145841.1:c.105C>T NP_001139313.1:p.Ser35=
NM_003282.3:c.105C>T NP_003273.1:p.Ser35=
NM_003282.4:c.105C>T MANE Select NP_003273.1:p.Ser35=
NM_001145829.2:c.105C>T NP_001139301.1:p.Ser35=
NM_001145841.2:c.105C>T NP_001139313.1:p.Ser35=