Canonical Allele Identifier: CA2499216960
Gene: TNNC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1289671
ClinVar RCV Id: RCV001714172
dbSNP Id: rs2153229907
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451198C>A , CM000665.2:g.52451198C>A GRCh38
NC_000003.11:g.52485214C>A , CM000665.1:g.52485214C>A GRCh37
NC_000003.10:g.52460254C>A NCBI36
NG_008963.1:g.7844G>T , LRG_378:g.7844G>T
NG_033112.1:g.691C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*77G>T MANE Select ENSP00000232975.3:n.*77G>T
ENST00000232975.7:c.*77G>T ENSP00000232975.3:n.*77G>T
NM_003280.2:c.*77G>T , LRG_378t1:c.*77G>T NP_003271.1:n.*77G>T
NM_003280.3:c.*77G>T MANE Select NP_003271.1:n.*77G>T
Search 100 bp 5'
Search 100 bp 3'