Canonical Allele Identifier: CA049990

Gene: TNNI3

Linked Data

• dbSNP Id: rs774167216
• ExAC: 19:55668369 T / C
• gnomAD v2: 19-55668369-T-C
• gnomAD v3: 19-55157001-T-C
• gnomAD v4: 19-55157001-T-C
• MyVariant Identifiers: chr19:g.55668369T>C (hg19) ; chr19:g.55157001T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55157001T>C , CM000681.2:g.55157001T>C	GRCh38
NC_000019.9:g.55668369T>C , CM000681.1:g.55668369T>C	GRCh37
NC_000019.8:g.60360181T>C	NCBI36
NG_007866.2:g.5732A>G , LRG_432:g.5732A>G
NG_032759.1:g.14722A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.108+49A>G MANE Select	ENSP00000341838.5:n.108+49A>G
ENST00000665070.1:c.108+49A>G	ENSP00000499482.1:n.108+49A>G
ENST00000344887.9:c.108+49A>G	ENSP00000341838.5:n.108+49A>G
ENST00000586446.1:n.299A>G
ENST00000586669.5:n.116+49A>G
ENST00000587176.5:n.292+49A>G
ENST00000587871.1:c.727+49A>G
ENST00000590463.1:n.280+49A>G
NM_000363.4:c.108+49A>G , LRG_432t1:c.108+49A>G	NP_000354.4:n.108+49A>G
NM_000363.5:c.108+49A>G MANE Select	NP_000354.4:n.108+49A>G