Canonical Allele Identifier: CA386700276
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110919143G>T , CM000674.2:g.110919143G>T GRCh38
NC_000012.11:g.111356947G>T , CM000674.1:g.111356947G>T GRCh37
NC_000012.10:g.109841330G>T NCBI36
NG_007554.1:g.6435C>A , LRG_393:g.6435C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.54C>A MANE Select ENSP00000228841.8:p.Phe18Leu
ENST00000663220.1:c.-4C>A ENSP00000499568.1:n.-4C>A
ENST00000228841.12:c.54C>A ENSP00000228841.7:p.Phe18Leu
ENST00000546404.1:n.247C>A
ENST00000548438.1:c.54C>A ENSP00000447154.1:p.Phe18Leu
NM_000432.3:c.54C>A , LRG_393t1:c.54C>A NP_000423.2:p.Phe18Leu
NM_000432.4:c.54C>A MANE Select NP_000423.2:p.Phe18Leu