Canonical Allele Identifier: CA2063070916

Gene: MYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110913316G= , CM000674.2:g.110913316G=	GRCh38
NC_000012.11:g.111351120G= , CM000674.1:g.111351120G=	GRCh37
NC_000012.10:g.109835503G=	NCBI36
NG_007554.1:g.12262C= , LRG_393:g.12262C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228841.15:c.283C= MANE Select	ENSP00000228841.8:p.Pro95=
ENST00000663220.1:c.226C=	ENSP00000499568.1:p.Pro76=
ENST00000228841.12:c.283C=	ENSP00000228841.7:p.Pro95=
ENST00000548438.1:c.241C=	ENSP00000447154.1:p.Pro81=
ENST00000549029.1:n.114C=
NM_000432.3:c.283C= , LRG_393t1:c.283C=	NP_000423.2:p.Pro95=
NM_000432.4:c.283C= MANE Select	NP_000423.2:p.Pro95=