Canonical Allele Identifier: CA407443116
Gene: TNNI3 HGNC NCBI

Linked Data

gnomAD v4: 19-55157102-A-C
MyVariant Identifiers: chr19:g.55668470A>C (hg19) chr19:g.55157102A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157102A>C , CM000681.2:g.55157102A>C GRCh38
NC_000019.9:g.55668470A>C , CM000681.1:g.55668470A>C GRCh37
NC_000019.8:g.60360282A>C NCBI36
NG_007866.2:g.5631T>G , LRG_432:g.5631T>G
NG_032759.1:g.14621T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.56T>G MANE Select ENSP00000341838.5:p.Ile19Ser
ENST00000665070.1:c.56T>G ENSP00000499482.1:p.Ile19Ser
ENST00000344887.9:c.56T>G ENSP00000341838.5:p.Ile19Ser
ENST00000586446.1:n.198T>G
ENST00000586669.5:n.64T>G
ENST00000587176.5:n.240T>G
ENST00000587871.1:c.675T>G
ENST00000590463.1:n.228T>G
NM_000363.4:c.56T>G , LRG_432t1:c.56T>G NP_000354.4:p.Ile19Ser
NM_000363.5:c.56T>G MANE Select NP_000354.4:p.Ile19Ser
Search 100 bp 5'
Search 100 bp 3'