Canonical Allele Identifier: CA2727312475
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs2136767138
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910911_110910912insATG , CM000674.2:g.110910911_110910912insATG GRCh38
NC_000012.11:g.111348715_111348716insATG , CM000674.1:g.111348715_111348716insATG GRCh37
NC_000012.10:g.109833098_109833099insATG NCBI36
NG_007554.1:g.14666_14667insCAT , LRG_393:g.14666_14667insCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*165_*166insCAT MANE Select ENSP00000228841.8:n.*165_*166insCAT
ENST00000663220.1:c.*165_*166insCAT ENSP00000499568.1:n.*165_*166insCAT
ENST00000228841.12:c.*165_*166insCAT ENSP00000228841.7:n.*165_*166insCAT
NM_000432.3:c.*165_*166insCAT , LRG_393t1:c.*165_*166insCAT NP_000423.2:n.*165_*166insCAT
NM_000432.4:c.*165_*166insCAT MANE Select NP_000423.2:n.*165_*166insCAT
Search 100 bp 5'
Search 100 bp 3'