Canonical Allele Identifier: CA508989396
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665449G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154081G>C , CM000681.2:g.55154081G>C GRCh38
NC_000019.9:g.55665449G>C , CM000681.1:g.55665449G>C GRCh37
NC_000019.8:g.60357261G>C NCBI36
NG_007866.2:g.8652C>G , LRG_432:g.8652C>G
NG_011829.2:g.158C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.498C>G MANE Select ENSP00000341838.5:p.Ser166=
ENST00000665070.1:c.531C>G ENSP00000499482.1:p.Ser177=
ENST00000344887.9:c.498C>G ENSP00000341838.5:p.Ser166=
ENST00000585806.5:n.497C>G
ENST00000588882.1:c.423C>G ENSP00000466729.1:p.Ser141=
ENST00000589864.1:n.326C>G
NM_000363.4:c.498C>G , LRG_432t1:c.498C>G NP_000354.4:p.Ser166=
NM_000363.5:c.498C>G MANE Select NP_000354.4:p.Ser166=
Search 100 bp 5'
Search 100 bp 3'