Canonical Allele Identifier: CA408524894
Gene: MYLK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.30407962C>G (hg19) chr20:g.31820159C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820159C>G , CM000682.2:g.31820159C>G GRCh38
NC_000020.10:g.30407962C>G , CM000682.1:g.30407962C>G GRCh37
NC_000020.9:g.29871623C>G NCBI36
NG_012847.1:g.5785C>G , LRG_392:g.5785C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.86C>G MANE Select ENSP00000365152.4:p.Pro29Arg
ENST00000375985.4:c.86C>G ENSP00000365152.4:p.Pro29Arg
ENST00000375994.6:c.86C>G ENSP00000365162.2:p.Pro29Arg
NM_033118.3:c.86C>G , LRG_392t1:c.86C>G NP_149109.1:p.Pro29Arg
XR_244155.1:n.251C>G
NM_033118.4:c.86C>G MANE Select NP_149109.1:p.Pro29Arg
Search 100 bp 5'
Search 100 bp 3'