Canonical Allele Identifier: CA441001805
Gene: MYOZ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120107139A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119185984A>T , CM000666.2:g.119185984A>T GRCh38
NC_000004.11:g.120107139A>T , CM000666.1:g.120107139A>T GRCh37
NC_000004.10:g.120326587A>T NCBI36
NG_029747.1:g.55201A>T , LRG_396:g.55201A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307128.6:c.579A>T MANE Select ENSP00000306997.6:p.Gly193=
ENST00000307128.5:c.579A>T ENSP00000306997.5:p.Gly193=
NM_016599.4:c.579A>T , LRG_396t1:c.579A>T NP_057683.1:p.Gly193=
NM_016599.5:c.579A>T MANE Select NP_057683.1:p.Gly193=
Search 100 bp 5'
Search 100 bp 3'