Canonical Allele Identifier: CA2063066389
Gene: MYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911021T= , CM000674.2:g.110911021T= GRCh38
NC_000012.11:g.111348825T= , CM000674.1:g.111348825T= GRCh37
NC_000012.10:g.109833208T= NCBI36
NG_007554.1:g.14557A= , LRG_393:g.14557A=

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*56A= MANE Select ENSP00000228841.8:n.*56A=
ENST00000663220.1:c.*56A= ENSP00000499568.1:n.*56A=
ENST00000228841.12:c.*56A= ENSP00000228841.7:n.*56A=
ENST00000548438.1:c.*56A= ENSP00000447154.1:n.*56A=
NM_000432.3:c.*56A= , LRG_393t1:c.*56A= NP_000423.2:n.*56A=
NM_000432.4:c.*56A= MANE Select NP_000423.2:n.*56A=