Canonical Allele Identifier: CA2063066695
Gene: MYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911103T= , CM000674.2:g.110911103T= GRCh38
NC_000012.11:g.111348907T= , CM000674.1:g.111348907T= GRCh37
NC_000012.10:g.109833290T= NCBI36
NG_007554.1:g.14475A= , LRG_393:g.14475A=

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.475A= MANE Select ENSP00000228841.8:p.Ile159=
ENST00000663220.1:c.418A= ENSP00000499568.1:p.Ile140=
ENST00000228841.12:c.475A= ENSP00000228841.7:p.Ile159=
ENST00000548438.1:c.433A= ENSP00000447154.1:p.Ile145=
NM_000432.3:c.475A= , LRG_393t1:c.475A= NP_000423.2:p.Ile159=
NM_000432.4:c.475A= MANE Select NP_000423.2:p.Ile159=