Canonical Allele Identifier: CA2620916393
Gene: MYL2 HGNC NCBI

Linked Data

gnomAD v4: 12-110911001-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911003del , CM000674.2:g.110911003del GRCh38
NC_000012.11:g.111348807del , CM000674.1:g.111348807del GRCh37
NC_000012.10:g.109833190del NCBI36
NG_007554.1:g.14576del , LRG_393:g.14576del

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*75del MANE Select ENSP00000228841.8:n.*75del
ENST00000663220.1:c.*75del ENSP00000499568.1:n.*75del
ENST00000228841.12:c.*75del ENSP00000228841.7:n.*75del
ENST00000548438.1:c.*75del ENSP00000447154.1:n.*75del
NM_000432.3:c.*75del , LRG_393t1:c.*75del NP_000423.2:n.*75del
NM_000432.4:c.*75del MANE Select NP_000423.2:n.*75del
Search 100 bp 5'
Search 100 bp 3'