Canonical Allele Identifier: CA6598773

Gene: MYG1

Linked Data

• dbSNP Id: rs376563652
• ExAC: 12:53700965 A / C
• gnomAD v2: 12-53700965-A-C
• gnomAD v3: 12-53307181-A-C
• gnomAD v4: 12-53307181-A-C
• MyVariant Identifiers: chr12:g.53700965A>C (hg19) ; chr12:g.53307181A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307181A>C , CM000674.2:g.53307181A>C	GRCh38
NC_000012.11:g.53700965A>C , CM000674.1:g.53700965A>C	GRCh37
NC_000012.10:g.51987232A>C	NCBI36
NG_016775.1:g.19448T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021640.3:c.*32A>C	NP_067653.3:n.*32A>C