Canonical Allele Identifier: CA2063072371
Gene: MYL2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.264G= MANE Select ENSP00000228841.8:p.Glu88=
ENST00000663220.1:c.207G= ENSP00000499568.1:p.Glu69=
ENST00000228841.12:c.264G= ENSP00000228841.7:p.Glu88=
ENST00000548438.1:c.222G= ENSP00000447154.1:p.Glu74=
ENST00000549029.1:n.95G=
NM_000432.3:c.264G= , LRG_393t1:c.264G= NP_000423.2:p.Glu88=
NM_000432.4:c.264G= MANE Select NP_000423.2:p.Glu88=