Canonical Allele Identifier: CA2727312926
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs2136767356

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911008_110911009del , CM000674.2:g.110911008_110911009del GRCh38
NC_000012.11:g.111348812_111348813del , CM000674.1:g.111348812_111348813del GRCh37
NC_000012.10:g.109833195_109833196del NCBI36
NG_007554.1:g.14569_14570del , LRG_393:g.14569_14570del

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*68_*69del MANE Select ENSP00000228841.8:n.*68_*69del
ENST00000663220.1:c.*68_*69del ENSP00000499568.1:n.*68_*69del
ENST00000228841.12:c.*68_*69del ENSP00000228841.7:n.*68_*69del
ENST00000548438.1:c.*68_*69del ENSP00000447154.1:n.*68_*69del
NM_000432.3:c.*68_*69del , LRG_393t1:c.*68_*69del NP_000423.2:n.*68_*69del
NM_000432.4:c.*68_*69del MANE Select NP_000423.2:n.*68_*69del