Canonical Allele Identifier: CA408525056
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30408041A>T (hg19) chr20:g.31820238A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820238A>T , CM000682.2:g.31820238A>T GRCh38
NC_000020.10:g.30408041A>T , CM000682.1:g.30408041A>T GRCh37
NC_000020.9:g.29871702A>T NCBI36
NG_012847.1:g.5864A>T , LRG_392:g.5864A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.165A>T MANE Select ENSP00000365152.4:p.Lys55Asn
ENST00000375985.4:c.165A>T ENSP00000365152.4:p.Lys55Asn
ENST00000375994.6:c.165A>T ENSP00000365162.2:p.Lys55Asn
NM_033118.3:c.165A>T , LRG_392t1:c.165A>T NP_149109.1:p.Lys55Asn
XR_244155.1:n.330A>T
NM_033118.4:c.165A>T MANE Select NP_149109.1:p.Lys55Asn
Search 100 bp 5'
Search 100 bp 3'