Canonical Allele Identifier: CA1047975582
Gene: TNNC1 HGNC NCBI

Linked Data

dbSNP Id: rs1706317308
gnomAD v3: 3-52451201-G-A
gnomAD v4: 3-52451201-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451201G>A , CM000665.2:g.52451201G>A GRCh38
NC_000003.11:g.52485217G>A , CM000665.1:g.52485217G>A GRCh37
NC_000003.10:g.52460257G>A NCBI36
NG_008963.1:g.7841C>T , LRG_378:g.7841C>T
NG_033112.1:g.694G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*74C>T MANE Select ENSP00000232975.3:n.*74C>T
ENST00000232975.7:c.*74C>T ENSP00000232975.3:n.*74C>T
NM_003280.2:c.*74C>T , LRG_378t1:c.*74C>T NP_003271.1:n.*74C>T
NM_003280.3:c.*74C>T MANE Select NP_003271.1:n.*74C>T
Search 100 bp 5'
Search 100 bp 3'