Canonical Allele Identifier: CA407439517

Gene: TNNI3

Linked Data

• dbSNP Id: rs2085696801
• MyVariant Identifiers: chr19:g.55663240T>C (hg19) ; chr19:g.55151872T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151872T>C , CM000681.2:g.55151872T>C	GRCh38
NC_000019.9:g.55663240T>C , CM000681.1:g.55663240T>C	GRCh37
NC_000019.8:g.60355052T>C	NCBI36
NG_007866.2:g.10861A>G , LRG_432:g.10861A>G
NG_011829.2:g.2367A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.595A>G MANE Select	ENSP00000341838.5:p.Ser199Gly
ENST00000665070.1:c.628A>G	ENSP00000499482.1:p.Ser210Gly
ENST00000344887.9:c.595A>G	ENSP00000341838.5:p.Ser199Gly
ENST00000585806.5:n.594A>G
ENST00000588882.1:c.520A>G	ENSP00000466729.1:p.Ser174Gly
ENST00000589864.1:n.423A>G
NM_000363.4:c.595A>G , LRG_432t1:c.595A>G	NP_000354.4:p.Ser199Gly
NM_000363.5:c.595A>G MANE Select	NP_000354.4:p.Ser199Gly