Canonical Allele Identifier: CA407439472

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663228C>G (hg19) ; chr19:g.55151860C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151860C>G , CM000681.2:g.55151860C>G	GRCh38
NC_000019.9:g.55663228C>G , CM000681.1:g.55663228C>G	GRCh37
NC_000019.8:g.60355040C>G	NCBI36
NG_007866.2:g.10873G>C , LRG_432:g.10873G>C
NG_011829.2:g.2379G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.607G>C MANE Select	ENSP00000341838.5:p.Gly203Arg
ENST00000665070.1:c.640G>C	ENSP00000499482.1:p.Gly214Arg
ENST00000344887.9:c.607G>C	ENSP00000341838.5:p.Gly203Arg
ENST00000585806.5:n.606G>C
ENST00000588882.1:c.532G>C	ENSP00000466729.1:p.Gly178Arg
ENST00000589864.1:n.435G>C
NM_000363.4:c.607G>C , LRG_432t1:c.607G>C	NP_000354.4:p.Gly203Arg
NM_000363.5:c.607G>C MANE Select	NP_000354.4:p.Gly203Arg