Canonical Allele Identifier: CA9803048
Gene: MYLK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765986
ClinVar RCV Id: RCV004055041
dbSNP Id: rs772673055

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824295A>G , CM000682.2:g.31824295A>G GRCh38
NC_000020.10:g.30412098A>G , CM000682.1:g.30412098A>G GRCh37
NC_000020.9:g.29875759A>G NCBI36
NG_012847.1:g.9921A>G , LRG_392:g.9921A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.915A>G MANE Select ENSP00000365152.4:p.Lys305=
ENST00000375985.4:c.915A>G ENSP00000365152.4:p.Lys305=
ENST00000375994.6:c.915A>G ENSP00000365162.2:p.Lys305=
NM_033118.3:c.915A>G , LRG_392t1:c.915A>G NP_149109.1:p.Lys305=
XR_244155.1:n.1281A>G
NM_033118.4:c.915A>G MANE Select NP_149109.1:p.Lys305=