Canonical Allele Identifier: CA310145163
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs546049287
MyVariant Identifiers: chr19:g.55663555C>G (hg19) chr19:g.55152187C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152187C>G , CM000681.2:g.55152187C>G GRCh38
NC_000019.9:g.55663555C>G , CM000681.1:g.55663555C>G GRCh37
NC_000019.8:g.60355367C>G NCBI36
NG_007866.2:g.10546G>C , LRG_432:g.10546G>C
NG_011829.2:g.2052G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-270G>C MANE Select ENSP00000341838.5:n.550-270G>C
ENST00000665070.1:c.583-270G>C ENSP00000499482.1:n.583-270G>C
ENST00000344887.9:c.550-270G>C ENSP00000341838.5:n.550-270G>C
ENST00000585806.5:n.549-270G>C
ENST00000588882.1:c.475-270G>C ENSP00000466729.1:n.475-270G>C
ENST00000589864.1:n.378-270G>C
NM_000363.4:c.550-270G>C , LRG_432t1:c.550-270G>C NP_000354.4:n.550-270G>C
NM_000363.5:c.550-270G>C MANE Select NP_000354.4:n.550-270G>C
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