Canonical Allele Identifier: CA74774931
Gene: TNNC1 HGNC NCBI

Linked Data

dbSNP Id: rs1043827011
gnomAD v2: 3-52485213-C-T
gnomAD v3: 3-52451197-C-T
gnomAD v4: 3-52451197-C-T
MyVariant Identifiers: chr3:g.52485213C>T (hg19) chr3:g.52451197C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451197C>T , CM000665.2:g.52451197C>T GRCh38
NC_000003.11:g.52485213C>T , CM000665.1:g.52485213C>T GRCh37
NC_000003.10:g.52460253C>T NCBI36
NG_008963.1:g.7845G>A , LRG_378:g.7845G>A
NG_033112.1:g.690C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*78G>A MANE Select ENSP00000232975.3:n.*78G>A
ENST00000232975.7:c.*78G>A ENSP00000232975.3:n.*78G>A
NM_003280.2:c.*78G>A , LRG_378t1:c.*78G>A NP_003271.1:n.*78G>A
NM_003280.3:c.*78G>A MANE Select NP_003271.1:n.*78G>A
Search 100 bp 5'
Search 100 bp 3'