Canonical Allele Identifier: CA2575173782
Gene: MYG1 HGNC NCBI

Linked Data

gnomAD v4: 12-53307175-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53307175T>C , CM000674.2:g.53307175T>C GRCh38
NC_000012.11:g.53700959T>C , CM000674.1:g.53700959T>C GRCh37
NC_000012.10:g.51987226T>C NCBI36
NG_016775.1:g.19454A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000267103.10:c.*26T>C MANE Select ENSP00000267103.5:n.*26T>C
ENST00000549488.5:c.*26T>C ENSP00000448433.1:n.*26T>C
NM_021640.3:c.*26T>C NP_067653.3:n.*26T>C
NM_021640.4:c.*26T>C MANE Select NP_067653.4:n.*26T>C
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