Canonical Allele Identifier: CA2666012922
Gene: TNNC1 HGNC NCBI

Linked Data

gnomAD v4: 3-52451211-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451211C>G , CM000665.2:g.52451211C>G GRCh38
NC_000003.11:g.52485227C>G , CM000665.1:g.52485227C>G GRCh37
NC_000003.10:g.52460267C>G NCBI36
NG_008963.1:g.7831G>C , LRG_378:g.7831G>C
NG_033112.1:g.704C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*64G>C MANE Select ENSP00000232975.3:n.*64G>C
ENST00000232975.7:c.*64G>C ENSP00000232975.3:n.*64G>C
NM_003280.2:c.*64G>C , LRG_378t1:c.*64G>C NP_003271.1:n.*64G>C
NM_003280.3:c.*64G>C MANE Select NP_003271.1:n.*64G>C
Search 100 bp 5'
Search 100 bp 3'