Canonical Allele Identifier: CA2036897342
Gene: MYG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53307180C= , CM000674.2:g.53307180C= GRCh38
NC_000012.11:g.53700964C= , CM000674.1:g.53700964C= GRCh37
NC_000012.10:g.51987231C= NCBI36
NG_016775.1:g.19449G=

Transcript Alleles

HGVS Amino-acid Change
NM_021640.3:c.*31C= NP_067653.3:n.*31C=