Canonical Allele Identifier: CA2619036425

Gene: MYG1

Linked Data

• gnomAD v4: 12-53307179-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307179C>A , CM000674.2:g.53307179C>A	GRCh38
NC_000012.11:g.53700963C>A , CM000674.1:g.53700963C>A	GRCh37
NC_000012.10:g.51987230C>A	NCBI36
NG_016775.1:g.19450G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021640.3:c.*30C>A	NP_067653.3:n.*30C>A