Canonical Allele Identifier: CA310148262

Gene: TNNI3

Linked Data

• dbSNP Id: rs766127569
• MyVariant Identifiers: chr19:g.55665372C>G (hg19) ; chr19:g.55154004C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154004C>G , CM000681.2:g.55154004C>G	GRCh38
NC_000019.9:g.55665372C>G , CM000681.1:g.55665372C>G	GRCh37
NC_000019.8:g.60357184C>G	NCBI36
NG_007866.2:g.8729G>C , LRG_432:g.8729G>C
NG_011829.2:g.235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+26G>C MANE Select	ENSP00000341838.5:n.549+26G>C
ENST00000665070.1:c.582+26G>C	ENSP00000499482.1:n.582+26G>C
ENST00000344887.9:c.549+26G>C	ENSP00000341838.5:n.549+26G>C
ENST00000585806.5:n.548+26G>C
ENST00000588882.1:c.474+26G>C	ENSP00000466729.1:n.474+26G>C
ENST00000589864.1:n.377+26G>C
NM_000363.4:c.549+26G>C , LRG_432t1:c.549+26G>C	NP_000354.4:n.549+26G>C
NM_000363.5:c.549+26G>C MANE Select	NP_000354.4:n.549+26G>C