Canonical Allele Identifier: CA2727312988
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs2136767368

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911016_110911017insAT , CM000674.2:g.110911016_110911017insAT GRCh38
NC_000012.11:g.111348820_111348821insAT , CM000674.1:g.111348820_111348821insAT GRCh37
NC_000012.10:g.109833203_109833204insAT NCBI36
NG_007554.1:g.14561_14562insAT , LRG_393:g.14561_14562insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.*60_*61insAT MANE Select ENSP00000228841.8:n.*60_*61insAT
ENST00000663220.1:c.*60_*61insAT ENSP00000499568.1:n.*60_*61insAT
ENST00000228841.12:c.*60_*61insAT ENSP00000228841.7:n.*60_*61insAT
ENST00000548438.1:c.*60_*61insAT ENSP00000447154.1:n.*60_*61insAT
NM_000432.3:c.*60_*61insAT , LRG_393t1:c.*60_*61insAT NP_000423.2:n.*60_*61insAT
NM_000432.4:c.*60_*61insAT MANE Select NP_000423.2:n.*60_*61insAT