Canonical Allele Identifier: CA022049
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 137688
ClinVar RCV Id: RCV000125568
dbSNP Id: rs587780968
gnomAD v2: 19-55663226-G-A
gnomAD v3: 19-55151858-G-A
gnomAD v4: 19-55151858-G-A
MyVariant Identifiers: chr19:g.55663226G>A (hg19) chr19:g.55151858G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151858G>A , CM000681.2:g.55151858G>A GRCh38
NC_000019.9:g.55663226G>A , CM000681.1:g.55663226G>A GRCh37
NC_000019.8:g.60355038G>A NCBI36
NG_007866.2:g.10875C>T , LRG_432:g.10875C>T
NG_011829.2:g.2381C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.609C>T MANE Select ENSP00000341838.5:p.Gly203=
ENST00000665070.1:c.642C>T ENSP00000499482.1:p.Gly214=
ENST00000344887.9:c.609C>T ENSP00000341838.5:p.Gly203=
ENST00000585806.5:n.608C>T
ENST00000588882.1:c.534C>T ENSP00000466729.1:p.Gly178=
ENST00000589864.1:n.437C>T
NM_000363.4:c.609C>T , LRG_432t1:c.609C>T NP_000354.4:p.Gly203=
NM_000363.5:c.609C>T MANE Select NP_000354.4:p.Gly203=
Search 100 bp 5'
Search 100 bp 3'