Canonical Allele Identifier: CA441001769
Gene: MYOZ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120107133A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119185978A>C , CM000666.2:g.119185978A>C GRCh38
NC_000004.11:g.120107133A>C , CM000666.1:g.120107133A>C GRCh37
NC_000004.10:g.120326581A>C NCBI36
NG_029747.1:g.55195A>C , LRG_396:g.55195A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307128.6:c.573A>C MANE Select ENSP00000306997.6:p.Pro191=
ENST00000307128.5:c.573A>C ENSP00000306997.5:p.Pro191=
NM_016599.4:c.573A>C , LRG_396t1:c.573A>C NP_057683.1:p.Pro191=
NM_016599.5:c.573A>C MANE Select NP_057683.1:p.Pro191=
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Search 100 bp 3'