Canonical Allele Identifier: CA358203274
Gene: MYOZ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119136566A>G , CM000666.2:g.119136566A>G GRCh38
NC_000004.11:g.120057721A>G , CM000666.1:g.120057721A>G GRCh37
NC_000004.10:g.120277169A>G NCBI36
NG_029747.1:g.5783A>G , LRG_396:g.5783A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307128.6:c.41A>G MANE Select ENSP00000306997.6:p.Gln14Arg
ENST00000307128.5:c.41A>G ENSP00000306997.5:p.Gln14Arg
NM_016599.4:c.41A>G , LRG_396t1:c.41A>G NP_057683.1:p.Gln14Arg
XM_006714234.2:c.41A>G XP_006714297.1:p.Gln14Arg
XM_006714234.4:c.41A>G XP_006714297.1:p.Gln14Arg
NM_016599.5:c.41A>G MANE Select NP_057683.1:p.Gln14Arg