Canonical Allele Identifier: CA358201386
Gene: MYOZ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120107137G>C (hg19) chr4:g.119185982G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119185982G>C , CM000666.2:g.119185982G>C GRCh38
NC_000004.11:g.120107137G>C , CM000666.1:g.120107137G>C GRCh37
NC_000004.10:g.120326585G>C NCBI36
NG_029747.1:g.55199G>C , LRG_396:g.55199G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307128.6:c.577G>C MANE Select ENSP00000306997.6:p.Gly193Arg
ENST00000307128.5:c.577G>C ENSP00000306997.5:p.Gly193Arg
NM_016599.4:c.577G>C , LRG_396t1:c.577G>C NP_057683.1:p.Gly193Arg
NM_016599.5:c.577G>C MANE Select NP_057683.1:p.Gly193Arg
Search 100 bp 5'
Search 100 bp 3'