Canonical Allele Identifier: CA1364863506
Gene: TNNC1 HGNC NCBI

Linked Data

dbSNP Id: rs1706317106
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*90G>A MANE Select ENSP00000232975.3:n.*90G>A
ENST00000232975.7:c.*90G>A ENSP00000232975.3:n.*90G>A
NM_003280.2:c.*90G>A , LRG_378t1:c.*90G>A NP_003271.1:n.*90G>A
NM_003280.3:c.*90G>A MANE Select NP_003271.1:n.*90G>A
Search 100 bp 5'
Search 100 bp 3'