Canonical Allele Identifier: CA310148503

Gene: TNNI3

Linked Data

• dbSNP Id: rs892779856
• gnomAD v2: 19-55665645-C-G
• gnomAD v3: 19-55154277-C-G
• gnomAD v4: 19-55154277-C-G
• MyVariant Identifiers: chr19:g.55665645C>G (hg19) ; chr19:g.55154277C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154277C>G , CM000681.2:g.55154277C>G	GRCh38
NC_000019.9:g.55665645C>G , CM000681.1:g.55665645C>G	GRCh37
NC_000019.8:g.60357457C>G	NCBI36
NG_007866.2:g.8456G>C , LRG_432:g.8456G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.373-71G>C MANE Select	ENSP00000341838.5:n.373-71G>C
ENST00000665070.1:c.406-71G>C	ENSP00000499482.1:n.406-71G>C
ENST00000344887.9:c.373-71G>C	ENSP00000341838.5:n.373-71G>C
ENST00000585806.5:n.372-71G>C
ENST00000586669.5:n.381-71G>C
ENST00000588882.1:c.298-71G>C	ENSP00000466729.1:n.298-71G>C
ENST00000589864.1:n.130G>C
NM_000363.4:c.373-71G>C , LRG_432t1:c.373-71G>C	NP_000354.4:n.373-71G>C
NM_000363.5:c.373-71G>C MANE Select	NP_000354.4:n.373-71G>C