Canonical Allele Identifier: CA358201360
Gene: MYOZ2 HGNC NCBI

Linked Data

dbSNP Id: rs1742284688
MyVariant Identifiers: chr4:g.120107129C>T (hg19) chr4:g.119185974C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119185974C>T , CM000666.2:g.119185974C>T GRCh38
NC_000004.11:g.120107129C>T , CM000666.1:g.120107129C>T GRCh37
NC_000004.10:g.120326577C>T NCBI36
NG_029747.1:g.55191C>T , LRG_396:g.55191C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307128.6:c.569C>T MANE Select ENSP00000306997.6:p.Thr190Ile
ENST00000307128.5:c.569C>T ENSP00000306997.5:p.Thr190Ile
NM_016599.4:c.569C>T , LRG_396t1:c.569C>T NP_057683.1:p.Thr190Ile
NM_016599.5:c.569C>T MANE Select NP_057683.1:p.Thr190Ile
Search 100 bp 5'
Search 100 bp 3'