Canonical Allele Identifier: CA633870567

Gene: TNNI3

Linked Data

• dbSNP Id: rs1245427255
• gnomAD v2: 19-55663639-T-C
• gnomAD v3: 19-55152271-T-C
• gnomAD v4: 19-55152271-T-C
• MyVariant Identifiers: chr19:g.55663639T>C (hg19) ; chr19:g.55152271T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152271T>C , CM000681.2:g.55152271T>C	GRCh38
NC_000019.9:g.55663639T>C , CM000681.1:g.55663639T>C	GRCh37
NC_000019.8:g.60355451T>C	NCBI36
NG_007866.2:g.10462A>G , LRG_432:g.10462A>G
NG_011829.2:g.1968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-354A>G MANE Select	ENSP00000341838.5:n.550-354A>G
ENST00000665070.1:c.583-354A>G	ENSP00000499482.1:n.583-354A>G
ENST00000344887.9:c.550-354A>G	ENSP00000341838.5:n.550-354A>G
ENST00000585806.5:n.549-354A>G
ENST00000588882.1:c.475-354A>G	ENSP00000466729.1:n.475-354A>G
ENST00000589864.1:n.378-354A>G
NM_000363.4:c.550-354A>G , LRG_432t1:c.550-354A>G	NP_000354.4:n.550-354A>G
NM_000363.5:c.550-354A>G MANE Select	NP_000354.4:n.550-354A>G