Canonical Allele Identifier: CA2666012870
Gene: TNNC1 HGNC NCBI

Linked Data

gnomAD v4: 3-52451185-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451185C>A , CM000665.2:g.52451185C>A GRCh38
NC_000003.11:g.52485201C>A , CM000665.1:g.52485201C>A GRCh37
NC_000003.10:g.52460241C>A NCBI36
NG_008963.1:g.7857G>T , LRG_378:g.7857G>T
NG_033112.1:g.678C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*90G>T MANE Select ENSP00000232975.3:n.*90G>T
ENST00000232975.7:c.*90G>T ENSP00000232975.3:n.*90G>T
NM_003280.2:c.*90G>T , LRG_378t1:c.*90G>T NP_003271.1:n.*90G>T
NM_003280.3:c.*90G>T MANE Select NP_003271.1:n.*90G>T
Search 100 bp 5'
Search 100 bp 3'