Canonical Allele Identifier: CA386696729
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911101G>C , CM000674.2:g.110911101G>C GRCh38
NC_000012.11:g.111348905G>C , CM000674.1:g.111348905G>C GRCh37
NC_000012.10:g.109833288G>C NCBI36
NG_007554.1:g.14477C>G , LRG_393:g.14477C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.477C>G MANE Select ENSP00000228841.8:p.Ile159Met
ENST00000663220.1:c.420C>G ENSP00000499568.1:p.Ile140Met
ENST00000228841.12:c.477C>G ENSP00000228841.7:p.Ile159Met
ENST00000548438.1:c.435C>G ENSP00000447154.1:p.Ile145Met
NM_000432.3:c.477C>G , LRG_393t1:c.477C>G NP_000423.2:p.Ile159Met
NM_000432.4:c.477C>G MANE Select NP_000423.2:p.Ile159Met