Canonical Allele Identifier: CA510173927
Gene: MYLK2 HGNC NCBI

Linked Data

gnomAD v4: 20-31820142-T-G
MyVariant Identifiers: chr20:g.30407945T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820142T>G , CM000682.2:g.31820142T>G GRCh38
NC_000020.10:g.30407945T>G , CM000682.1:g.30407945T>G GRCh37
NC_000020.9:g.29871606T>G NCBI36
NG_012847.1:g.5768T>G , LRG_392:g.5768T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.69T>G MANE Select ENSP00000365152.4:p.Gly23=
ENST00000375985.4:c.69T>G ENSP00000365152.4:p.Gly23=
ENST00000375994.6:c.69T>G ENSP00000365162.2:p.Gly23=
NM_033118.3:c.69T>G , LRG_392t1:c.69T>G NP_149109.1:p.Gly23=
XR_244155.1:n.234T>G
NM_033118.4:c.69T>G MANE Select NP_149109.1:p.Gly23=
Search 100 bp 5'
Search 100 bp 3'