Canonical Allele Identifier: CA883722686

Gene: TNNI3

Linked Data

• dbSNP Id: rs1409570098
• MyVariant Identifiers: chr19:g.55665675G>C (hg19) ; chr19:g.55154307G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154307G>C , CM000681.2:g.55154307G>C	GRCh38
NC_000019.9:g.55665675G>C , CM000681.1:g.55665675G>C	GRCh37
NC_000019.8:g.60357487G>C	NCBI36
NG_007866.2:g.8426C>G , LRG_432:g.8426C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.373-101C>G MANE Select	ENSP00000341838.5:n.373-101C>G
ENST00000665070.1:c.406-101C>G	ENSP00000499482.1:n.406-101C>G
ENST00000344887.9:c.373-101C>G	ENSP00000341838.5:n.373-101C>G
ENST00000585806.5:n.372-101C>G
ENST00000586669.5:n.381-101C>G
ENST00000587176.5:n.990C>G
ENST00000588882.1:c.298-101C>G	ENSP00000466729.1:n.298-101C>G
ENST00000589864.1:n.100C>G
NM_000363.4:c.373-101C>G , LRG_432t1:c.373-101C>G	NP_000354.4:n.373-101C>G
NM_000363.5:c.373-101C>G MANE Select	NP_000354.4:n.373-101C>G