Canonical Allele Identifier: CA2763275921
Gene: MYOZ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119136454A>G , CM000666.2:g.119136454A>G GRCh38
NC_000004.11:g.120057609A>G , CM000666.1:g.120057609A>G GRCh37
NC_000004.10:g.120277057A>G NCBI36
NG_029747.1:g.5671A>G , LRG_396:g.5671A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307128.6:c.-14-58A>G MANE Select ENSP00000306997.6:n.-14-58A>G
ENST00000307128.5:c.-14-58A>G ENSP00000306997.5:n.-14-58A>G
NM_016599.4:c.-14-58A>G , LRG_396t1:c.-14-58A>G NP_057683.1:n.-14-58A>G
XM_006714234.2:c.-14-58A>G XP_006714297.1:n.-14-58A>G
XM_006714234.4:c.-14-58A>G XP_006714297.1:n.-14-58A>G
NM_016599.5:c.-14-58A>G MANE Select NP_057683.1:n.-14-58A>G