Canonical Allele Identifier: CA2063072366

Gene: MYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110914187C= , CM000674.2:g.110914187C=	GRCh38
NC_000012.11:g.111351991C= , CM000674.1:g.111351991C=	GRCh37
NC_000012.10:g.109836374C=	NCBI36
NG_007554.1:g.11391G= , LRG_393:g.11391G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000228841.15:c.273G= MANE Select	ENSP00000228841.8:p.Lys91=
ENST00000663220.1:c.216G=	ENSP00000499568.1:p.Lys72=
ENST00000228841.12:c.273G=	ENSP00000228841.7:p.Lys91=
ENST00000548438.1:c.231G=	ENSP00000447154.1:p.Lys77=
ENST00000549029.1:n.104G=
NM_000432.3:c.273G= , LRG_393t1:c.273G=	NP_000423.2:p.Lys91=
NM_000432.4:c.273G= MANE Select	NP_000423.2:p.Lys91=