Canonical Allele Identifier: CA2063066157
Gene: MYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910913A= , CM000674.2:g.110910913A= GRCh38
NC_000012.11:g.111348717A= , CM000674.1:g.111348717A= GRCh37
NC_000012.10:g.109833100A= NCBI36
NG_007554.1:g.14665T= , LRG_393:g.14665T=

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*164T= MANE Select ENSP00000228841.8:n.*164T=
ENST00000663220.1:c.*164T= ENSP00000499568.1:n.*164T=
ENST00000228841.12:c.*164T= ENSP00000228841.7:n.*164T=
NM_000432.3:c.*164T= , LRG_393t1:c.*164T= NP_000423.2:n.*164T=
NM_000432.4:c.*164T= MANE Select NP_000423.2:n.*164T=