Canonical Allele Identifier: CA310148753

Gene: TNNI3

Linked Data

• dbSNP Id: rs372999288
• gnomAD v4: 19-55154671-G-A
• MyVariant Identifiers: chr19:g.55666039G>A (hg19) ; chr19:g.55154671G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154671G>A , CM000681.2:g.55154671G>A	GRCh38
NC_000019.9:g.55666039G>A , CM000681.1:g.55666039G>A	GRCh37
NC_000019.8:g.60357851G>A	NCBI36
NG_007866.2:g.8062C>T , LRG_432:g.8062C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.372+70C>T MANE Select	ENSP00000341838.5:n.372+70C>T
ENST00000665070.1:c.405+37C>T	ENSP00000499482.1:n.405+37C>T
ENST00000344887.9:c.372+70C>T	ENSP00000341838.5:n.372+70C>T
ENST00000585806.5:n.371+70C>T
ENST00000586669.5:n.380+70C>T
ENST00000587176.5:n.626C>T
ENST00000588882.1:c.297+70C>T	ENSP00000466729.1:n.297+70C>T
NM_000363.4:c.372+70C>T , LRG_432t1:c.372+70C>T	NP_000354.4:n.372+70C>T
NM_000363.5:c.372+70C>T MANE Select	NP_000354.4:n.372+70C>T