Canonical Allele Identifier: CA5815305

Gene: TNNI2

Linked Data

• dbSNP Id: rs770212007
• ExAC: 11:1862681 C / T
• gnomAD v4: 11-1841451-C-T
• MyVariant Identifiers: chr11:g.1862681C>T (hg19) ; chr11:g.1841451C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841451C>T , CM000673.2:g.1841451C>T	GRCh38
NC_000011.9:g.1862681C>T , CM000673.1:g.1862681C>T	GRCh37
NC_000011.8:g.1819257C>T	NCBI36
NG_011621.1:g.7449C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.454-5C>T MANE Select	ENSP00000371336.1:n.454-5C>T
ENST00000252898.11:c.454-5C>T	ENSP00000252898.7:n.454-5C>T
ENST00000381905.3:c.454-5C>T	ENSP00000371330.3:n.454-5C>T
ENST00000381906.5:c.454-5C>T	ENSP00000371331.1:n.454-5C>T
ENST00000381911.5:c.454-5C>T	ENSP00000371336.1:n.454-5C>T
ENST00000617947.4:c.454-5C>T	ENSP00000481242.1:n.454-5C>T
NM_001145829.1:c.454-5C>T	NP_001139301.1:n.454-5C>T
NM_001145841.1:c.454-5C>T	NP_001139313.1:n.454-5C>T
NM_003282.3:c.454-5C>T	NP_003273.1:n.454-5C>T
NM_003282.4:c.454-5C>T MANE Select	NP_003273.1:n.454-5C>T
NM_001145829.2:c.454-5C>T	NP_001139301.1:n.454-5C>T
NM_001145841.2:c.454-5C>T	NP_001139313.1:n.454-5C>T