Canonical Allele Identifier: CA353168547
Gene: TNNC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 537985
ClinVar RCV Id: RCV000647107
dbSNP Id: rs1553651742
MyVariant Identifiers: chr3:g.52486167T>C (hg19) chr3:g.52452151T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52452151T>C , CM000665.2:g.52452151T>C GRCh38
NC_000003.11:g.52486167T>C , CM000665.1:g.52486167T>C GRCh37
NC_000003.10:g.52461207T>C NCBI36
NG_008963.1:g.6891A>G , LRG_378:g.6891A>G
NG_033112.1:g.1644T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.157A>G MANE Select ENSP00000232975.3:p.Thr53Ala
ENST00000232975.7:c.157A>G ENSP00000232975.3:p.Thr53Ala
ENST00000496590.1:c.25A>G ENSP00000420596.1:p.Thr9Ala
NM_003280.2:c.157A>G , LRG_378t1:c.157A>G NP_003271.1:p.Thr53Ala
NM_003280.3:c.157A>G MANE Select NP_003271.1:p.Thr53Ala
Search 100 bp 5'
Search 100 bp 3'