Canonical Allele Identifier: CA633872396

Gene: TNNI3

Linked Data

• dbSNP Id: rs1313263655
• gnomAD v2: 19-55668996-G-A
• gnomAD v4: 19-55157628-G-A
• MyVariant Identifiers: chr19:g.55668996G>A (hg19) ; chr19:g.55157628G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55157628G>A , CM000681.2:g.55157628G>A	GRCh38
NC_000019.9:g.55668996G>A , CM000681.1:g.55668996G>A	GRCh37
NC_000019.8:g.60360808G>A	NCBI36
NG_007866.2:g.5105C>T , LRG_432:g.5105C>T
NG_032759.1:g.14095C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.-39C>T MANE Select	ENSP00000341838.5:n.-39C>T
ENST00000665070.1:c.-39C>T	ENSP00000499482.1:n.-39C>T
ENST00000344887.9:c.-39C>T	ENSP00000341838.5:n.-39C>T
ENST00000586446.1:n.105C>T
ENST00000587176.5:n.146C>T
ENST00000587871.1:c.582C>T
ENST00000590463.1:n.89C>T
NM_000363.4:c.-39C>T , LRG_432t1:c.-39C>T	NP_000354.4:n.-39C>T
NM_000363.5:c.-39C>T MANE Select	NP_000354.4:n.-39C>T