Canonical Allele Identifier: CA2727312523
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs2136767165

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910915_110910916insCTC , CM000674.2:g.110910915_110910916insCTC GRCh38
NC_000012.11:g.111348719_111348720insCTC , CM000674.1:g.111348719_111348720insCTC GRCh37
NC_000012.10:g.109833102_109833103insCTC NCBI36
NG_007554.1:g.14662_14663insGAG , LRG_393:g.14662_14663insGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.*161_*162insGAG MANE Select ENSP00000228841.8:n.*161_*162insGAG
ENST00000663220.1:c.*161_*162insGAG ENSP00000499568.1:n.*161_*162insGAG
ENST00000228841.12:c.*161_*162insGAG ENSP00000228841.7:n.*161_*162insGAG
NM_000432.3:c.*161_*162insGAG , LRG_393t1:c.*161_*162insGAG NP_000423.2:n.*161_*162insGAG
NM_000432.4:c.*161_*162insGAG MANE Select NP_000423.2:n.*161_*162insGAG