Canonical Allele Identifier: CA407443092
Gene: TNNI3 HGNC NCBI

Linked Data

gnomAD v4: 19-55157097-G-C
MyVariant Identifiers: chr19:g.55668465G>C (hg19) chr19:g.55157097G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157097G>C , CM000681.2:g.55157097G>C GRCh38
NC_000019.9:g.55668465G>C , CM000681.1:g.55668465G>C GRCh37
NC_000019.8:g.60360277G>C NCBI36
NG_007866.2:g.5636C>G , LRG_432:g.5636C>G
NG_032759.1:g.14626C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.61C>G MANE Select ENSP00000341838.5:p.Arg21Gly
ENST00000665070.1:c.61C>G ENSP00000499482.1:p.Arg21Gly
ENST00000344887.9:c.61C>G ENSP00000341838.5:p.Arg21Gly
ENST00000586446.1:n.203C>G
ENST00000586669.5:n.69C>G
ENST00000587176.5:n.245C>G
ENST00000587871.1:c.680C>G
ENST00000590463.1:n.233C>G
NM_000363.4:c.61C>G , LRG_432t1:c.61C>G NP_000354.4:p.Arg21Gly
NM_000363.5:c.61C>G MANE Select NP_000354.4:p.Arg21Gly
Search 100 bp 5'
Search 100 bp 3'