Canonical Allele Identifier: CA358202079

Gene: MYOZ2

Linked Data

• MyVariant Identifiers: chr4:g.120107220G>T (hg19) ; chr4:g.119186065G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119186065G>T , CM000666.2:g.119186065G>T	GRCh38
NC_000004.11:g.120107220G>T , CM000666.1:g.120107220G>T	GRCh37
NC_000004.10:g.120326668G>T	NCBI36
NG_029747.1:g.55282G>T , LRG_396:g.55282G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307128.6:c.660G>T MANE Select	ENSP00000306997.6:p.Met220Ile
ENST00000307128.5:c.660G>T	ENSP00000306997.5:p.Met220Ile
NM_016599.4:c.660G>T , LRG_396t1:c.660G>T	NP_057683.1:p.Met220Ile
NM_016599.5:c.660G>T MANE Select	NP_057683.1:p.Met220Ile