Canonical Allele Identifier: CA2063072736

Gene: MYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110914282T= , CM000674.2:g.110914282T=	GRCh38
NC_000012.11:g.111352086T= , CM000674.1:g.111352086T=	GRCh37
NC_000012.10:g.109836469T=	NCBI36
NG_007554.1:g.11296A= , LRG_393:g.11296A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228841.15:c.178A= MANE Select	ENSP00000228841.8:p.Asn60=
ENST00000663220.1:c.121A=	ENSP00000499568.1:p.Asn41=
ENST00000228841.12:c.178A=	ENSP00000228841.7:p.Asn60=
ENST00000548438.1:c.136A=	ENSP00000447154.1:p.Asn46=
ENST00000549029.1:n.9A=
NM_000432.3:c.178A= , LRG_393t1:c.178A=	NP_000423.2:p.Asn60=
NM_000432.4:c.178A= MANE Select	NP_000423.2:p.Asn60=