Canonical Allele Identifier: CA386696732
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911102A>T , CM000674.2:g.110911102A>T GRCh38
NC_000012.11:g.111348906A>T , CM000674.1:g.111348906A>T GRCh37
NC_000012.10:g.109833289A>T NCBI36
NG_007554.1:g.14476T>A , LRG_393:g.14476T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.476T>A MANE Select ENSP00000228841.8:p.Ile159Asn
ENST00000663220.1:c.419T>A ENSP00000499568.1:p.Ile140Asn
ENST00000228841.12:c.476T>A ENSP00000228841.7:p.Ile159Asn
ENST00000548438.1:c.434T>A ENSP00000447154.1:p.Ile145Asn
NM_000432.3:c.476T>A , LRG_393t1:c.476T>A NP_000423.2:p.Ile159Asn
NM_000432.4:c.476T>A MANE Select NP_000423.2:p.Ile159Asn