Canonical Allele Identifier: CA407439660

Gene: TNNI3

Linked Data

• dbSNP Id: rs1599907619
• MyVariant Identifiers: chr19:g.55663272A>C (hg19) ; chr19:g.55151904A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151904A>C , CM000681.2:g.55151904A>C	GRCh38
NC_000019.9:g.55663272A>C , CM000681.1:g.55663272A>C	GRCh37
NC_000019.8:g.60355084A>C	NCBI36
NG_007866.2:g.10829T>G , LRG_432:g.10829T>G
NG_011829.2:g.2335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.563T>G MANE Select	ENSP00000341838.5:p.Val188Gly
ENST00000665070.1:c.596T>G	ENSP00000499482.1:p.Val199Gly
ENST00000344887.9:c.563T>G	ENSP00000341838.5:p.Val188Gly
ENST00000585806.5:n.562T>G
ENST00000588882.1:c.488T>G	ENSP00000466729.1:p.Val163Gly
ENST00000589864.1:n.391T>G
NM_000363.4:c.563T>G , LRG_432t1:c.563T>G	NP_000354.4:p.Val188Gly
NM_000363.5:c.563T>G MANE Select	NP_000354.4:p.Val188Gly