Canonical Allele Identifier: CA386696720
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911097G>A , CM000674.2:g.110911097G>A GRCh38
NC_000012.11:g.111348901G>A , CM000674.1:g.111348901G>A GRCh37
NC_000012.10:g.109833284G>A NCBI36
NG_007554.1:g.14481C>T , LRG_393:g.14481C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.481C>T MANE Select ENSP00000228841.8:p.His161Tyr
ENST00000663220.1:c.424C>T ENSP00000499568.1:p.His142Tyr
ENST00000228841.12:c.481C>T ENSP00000228841.7:p.His161Tyr
ENST00000548438.1:c.439C>T ENSP00000447154.1:p.His147Tyr
NM_000432.3:c.481C>T , LRG_393t1:c.481C>T NP_000423.2:p.His161Tyr
NM_000432.4:c.481C>T MANE Select NP_000423.2:p.His161Tyr