Canonical Allele Identifier: CA1488821431
Gene: MYOZ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119185907T= , CM000666.2:g.119185907T= GRCh38
NC_000004.11:g.120107062T= , CM000666.1:g.120107062T= GRCh37
NC_000004.10:g.120326510T= NCBI36
NG_029747.1:g.55124T= , LRG_396:g.55124T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307128.6:c.561-59T= MANE Select ENSP00000306997.6:n.561-59T=
ENST00000307128.5:c.561-59T= ENSP00000306997.5:n.561-59T=
NM_016599.4:c.561-59T= , LRG_396t1:c.561-59T= NP_057683.1:n.561-59T=
NM_016599.5:c.561-59T= MANE Select NP_057683.1:n.561-59T=