Canonical Allele Identifier: CA997261527

Gene: TNNI3

Linked Data

• dbSNP Id: rs2147283850
• gnomAD v3: 19-55154946-A-G
• gnomAD v4: 19-55154946-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154946A>G , CM000681.2:g.55154946A>G	GRCh38
NC_000019.9:g.55666314A>G , CM000681.1:g.55666314A>G	GRCh37
NC_000019.8:g.60358126A>G	NCBI36
NG_007866.2:g.7787T>C , LRG_432:g.7787T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-116T>C MANE Select	ENSP00000341838.5:n.283-116T>C
ENST00000665070.1:c.283-116T>C	ENSP00000499482.1:n.283-116T>C
ENST00000344887.9:c.283-116T>C	ENSP00000341838.5:n.283-116T>C
ENST00000585806.5:n.282-116T>C
ENST00000586669.5:n.291-116T>C
ENST00000587176.5:n.467-116T>C
ENST00000587871.1:c.902-116T>C
ENST00000588882.1:c.208-116T>C	ENSP00000466729.1:n.208-116T>C
ENST00000590463.1:n.455-116T>C
NM_000363.4:c.283-116T>C , LRG_432t1:c.283-116T>C	NP_000354.4:n.283-116T>C
NM_000363.5:c.283-116T>C MANE Select	NP_000354.4:n.283-116T>C