Canonical Allele Identifier: CA508989485
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs111841348
gnomAD v4: 19-55154738-C-T
MyVariant Identifiers: chr19:g.55666106C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154738C>T , CM000681.2:g.55154738C>T GRCh38
NC_000019.9:g.55666106C>T , CM000681.1:g.55666106C>T GRCh37
NC_000019.8:g.60357918C>T NCBI36
NG_007866.2:g.7995G>A , LRG_432:g.7995G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.372+3G>A MANE Select ENSP00000341838.5:n.372+3G>A
ENST00000665070.1:c.375G>A ENSP00000499482.1:p.Val125=
ENST00000344887.9:c.372+3G>A ENSP00000341838.5:n.372+3G>A
ENST00000585806.5:n.371+3G>A
ENST00000586669.5:n.380+3G>A
ENST00000587176.5:n.559G>A
ENST00000588882.1:c.297+3G>A ENSP00000466729.1:n.297+3G>A
NM_000363.4:c.372+3G>A , LRG_432t1:c.372+3G>A NP_000354.4:n.372+3G>A
NM_000363.5:c.372+3G>A MANE Select NP_000354.4:n.372+3G>A
Search 100 bp 5'
Search 100 bp 3'