Canonical Allele Identifier: CA2063066181
Gene: MYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910921A= , CM000674.2:g.110910921A= GRCh38
NC_000012.11:g.111348725A= , CM000674.1:g.111348725A= GRCh37
NC_000012.10:g.109833108A= NCBI36
NG_007554.1:g.14657T= , LRG_393:g.14657T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.*156T= MANE Select ENSP00000228841.8:n.*156T=
ENST00000663220.1:c.*156T= ENSP00000499568.1:n.*156T=
ENST00000228841.12:c.*156T= ENSP00000228841.7:n.*156T=
ENST00000548438.1:c.*156T= ENSP00000447154.1:n.*156T=
NM_000432.3:c.*156T= , LRG_393t1:c.*156T= NP_000423.2:n.*156T=
NM_000432.4:c.*156T= MANE Select NP_000423.2:n.*156T=