Canonical Allele Identifier: CA655200722
Gene: MYG1 HGNC NCBI

Linked Data

gnomAD v4: 12-53307176-G-T
COSMIC: COSN21430483
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53307176G>T , CM000674.2:g.53307176G>T GRCh38
NC_000012.11:g.53700960G>T , CM000674.1:g.53700960G>T GRCh37
NC_000012.10:g.51987227G>T NCBI36
NG_016775.1:g.19453C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000267103.10:c.*27G>T MANE Select ENSP00000267103.5:n.*27G>T
ENST00000549488.5:c.*27G>T ENSP00000448433.1:n.*27G>T
NM_021640.3:c.*27G>T NP_067653.3:n.*27G>T
NM_021640.4:c.*27G>T MANE Select NP_067653.4:n.*27G>T
Search 100 bp 5'
Search 100 bp 3'