Canonical Allele Identifier: CA2063066182

Gene: MYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110910923A= , CM000674.2:g.110910923A=	GRCh38
NC_000012.11:g.111348727A= , CM000674.1:g.111348727A=	GRCh37
NC_000012.10:g.109833110A=	NCBI36
NG_007554.1:g.14655T= , LRG_393:g.14655T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000228841.15:c.*154T= MANE Select	ENSP00000228841.8:n.*154T=
ENST00000663220.1:c.*154T=	ENSP00000499568.1:n.*154T=
ENST00000228841.12:c.*154T=	ENSP00000228841.7:n.*154T=
ENST00000548438.1:c.*154T=	ENSP00000447154.1:n.*154T=
NM_000432.3:c.*154T= , LRG_393t1:c.*154T=	NP_000423.2:n.*154T=
NM_000432.4:c.*154T= MANE Select	NP_000423.2:n.*154T=