Canonical Allele Identifier: CA633872400

Gene: TNNI3

Linked Data

• dbSNP Id: rs1242688089
• gnomAD v2: 19-55669002-G-C
• gnomAD v4: 19-55157634-G-C
• MyVariant Identifiers: chr19:g.55669002G>C (hg19) ; chr19:g.55157634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55157634G>C , CM000681.2:g.55157634G>C	GRCh38
NC_000019.9:g.55669002G>C , CM000681.1:g.55669002G>C	GRCh37
NC_000019.8:g.60360814G>C	NCBI36
NG_007866.2:g.5099C>G , LRG_432:g.5099C>G
NG_032759.1:g.14089C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.-45C>G MANE Select	ENSP00000341838.5:n.-45C>G
ENST00000665070.1:c.-45C>G	ENSP00000499482.1:n.-45C>G
ENST00000344887.9:c.-45C>G	ENSP00000341838.5:n.-45C>G
ENST00000586446.1:n.99C>G
ENST00000587176.5:n.140C>G
ENST00000587871.1:c.576C>G
ENST00000590463.1:n.83C>G
NM_000363.4:c.-45C>G , LRG_432t1:c.-45C>G	NP_000354.4:n.-45C>G
NM_000363.5:c.-45C>G MANE Select	NP_000354.4:n.-45C>G