Canonical Allele Identifier: CA2727312828
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs2136767326

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910990_110910994del , CM000674.2:g.110910990_110910994del GRCh38
NC_000012.11:g.111348794_111348798del , CM000674.1:g.111348794_111348798del GRCh37
NC_000012.10:g.109833177_109833181del NCBI36
NG_007554.1:g.14584_14588del , LRG_393:g.14584_14588del

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*83_*87del MANE Select ENSP00000228841.8:n.*83_*87del
ENST00000663220.1:c.*83_*87del ENSP00000499568.1:n.*83_*87del
ENST00000228841.12:c.*83_*87del ENSP00000228841.7:n.*83_*87del
ENST00000548438.1:c.*83_*87del ENSP00000447154.1:n.*83_*87del
NM_000432.3:c.*83_*87del , LRG_393t1:c.*83_*87del NP_000423.2:n.*83_*87del
NM_000432.4:c.*83_*87del MANE Select NP_000423.2:n.*83_*87del