Canonical Allele Identifier: CA2063066146
Gene: MYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910911C= , CM000674.2:g.110910911C= GRCh38
NC_000012.11:g.111348715C= , CM000674.1:g.111348715C= GRCh37
NC_000012.10:g.109833098C= NCBI36
NG_007554.1:g.14667G= , LRG_393:g.14667G=

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*166G= MANE Select ENSP00000228841.8:n.*166G=
ENST00000663220.1:c.*166G= ENSP00000499568.1:n.*166G=
ENST00000228841.12:c.*166G= ENSP00000228841.7:n.*166G=
NM_000432.3:c.*166G= , LRG_393t1:c.*166G= NP_000423.2:n.*166G=
NM_000432.4:c.*166G= MANE Select NP_000423.2:n.*166G=