Canonical Allele Identifier: CA386698661

Gene: MYL2

Linked Data

• COSMIC: COSM935029
• MyVariant Identifiers: chr12:g.111352000C>A (hg19) ; chr12:g.110914196C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110914196C>A , CM000674.2:g.110914196C>A	GRCh38
NC_000012.11:g.111352000C>A , CM000674.1:g.111352000C>A	GRCh37
NC_000012.10:g.109836383C>A	NCBI36
NG_007554.1:g.11382G>T , LRG_393:g.11382G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000228841.15:c.264G>T MANE Select	ENSP00000228841.8:p.Glu88Asp
ENST00000663220.1:c.207G>T	ENSP00000499568.1:p.Glu69Asp
ENST00000228841.12:c.264G>T	ENSP00000228841.7:p.Glu88Asp
ENST00000548438.1:c.222G>T	ENSP00000447154.1:p.Glu74Asp
ENST00000549029.1:n.95G>T
NM_000432.3:c.264G>T , LRG_393t1:c.264G>T	NP_000423.2:p.Glu88Asp
NM_000432.4:c.264G>T MANE Select	NP_000423.2:p.Glu88Asp