Canonical Allele Identifier: CA919173732

Gene: MYL2

Linked Data

• dbSNP Id: rs1555257765

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110913199_110913200insC , CM000674.2:g.110913199_110913200insC	GRCh38
NC_000012.11:g.111351003_111351004insC , CM000674.1:g.111351003_111351004insC	GRCh37
NC_000012.10:g.109835386_109835387insC	NCBI36
NG_007554.1:g.12378_12379insG , LRG_393:g.12378_12379insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228841.15:c.353+46_353+47insG MANE Select	ENSP00000228841.8:n.353+46_353+47insG
ENST00000663220.1:c.296+46_296+47insG	ENSP00000499568.1:n.296+46_296+47insG
ENST00000228841.12:c.353+46_353+47insG	ENSP00000228841.7:n.353+46_353+47insG
ENST00000548438.1:c.311+46_311+47insG	ENSP00000447154.1:n.311+46_311+47insG
ENST00000549029.1:n.230_231insG
NM_000432.3:c.353+46_353+47insG , LRG_393t1:c.353+46_353+47insG	NP_000423.2:n.353+46_353+47insG
NM_000432.4:c.353+46_353+47insG MANE Select	NP_000423.2:n.353+46_353+47insG