Canonical Allele Identifier: CA386696727
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911100T>C , CM000674.2:g.110911100T>C GRCh38
NC_000012.11:g.111348904T>C , CM000674.1:g.111348904T>C GRCh37
NC_000012.10:g.109833287T>C NCBI36
NG_007554.1:g.14478A>G , LRG_393:g.14478A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.478A>G MANE Select ENSP00000228841.8:p.Thr160Ala
ENST00000663220.1:c.421A>G ENSP00000499568.1:p.Thr141Ala
ENST00000228841.12:c.478A>G ENSP00000228841.7:p.Thr160Ala
ENST00000548438.1:c.436A>G ENSP00000447154.1:p.Thr146Ala
NM_000432.3:c.478A>G , LRG_393t1:c.478A>G NP_000423.2:p.Thr160Ala
NM_000432.4:c.478A>G MANE Select NP_000423.2:p.Thr160Ala