Canonical Allele Identifier: CA1488799954
Gene: MYOZ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119136488A= , CM000666.2:g.119136488A= GRCh38
NC_000004.11:g.120057643A= , CM000666.1:g.120057643A= GRCh37
NC_000004.10:g.120277091A= NCBI36
NG_029747.1:g.5705A= , LRG_396:g.5705A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307128.6:c.-14-24A= MANE Select ENSP00000306997.6:n.-14-24A=
ENST00000307128.5:c.-14-24A= ENSP00000306997.5:n.-14-24A=
NM_016599.4:c.-14-24A= , LRG_396t1:c.-14-24A= NP_057683.1:n.-14-24A=
XM_006714234.2:c.-14-24A= XP_006714297.1:n.-14-24A=
XM_006714234.4:c.-14-24A= XP_006714297.1:n.-14-24A=
NM_016599.5:c.-14-24A= MANE Select NP_057683.1:n.-14-24A=