Canonical Allele Identifier: CA510173918
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30407936A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820133A>C , CM000682.2:g.31820133A>C GRCh38
NC_000020.10:g.30407936A>C , CM000682.1:g.30407936A>C GRCh37
NC_000020.9:g.29871597A>C NCBI36
NG_012847.1:g.5759A>C , LRG_392:g.5759A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.60A>C MANE Select ENSP00000365152.4:p.Ala20=
ENST00000375985.4:c.60A>C ENSP00000365152.4:p.Ala20=
ENST00000375994.6:c.60A>C ENSP00000365162.2:p.Ala20=
NM_033118.3:c.60A>C , LRG_392t1:c.60A>C NP_149109.1:p.Ala20=
XR_244155.1:n.225A>C
NM_033118.4:c.60A>C MANE Select NP_149109.1:p.Ala20=
Search 100 bp 5'
Search 100 bp 3'