Canonical Allele Identifier: CA408524868
Gene: MYLK2 HGNC NCBI

Linked Data

gnomAD v4: 20-31820146-A-G
MyVariant Identifiers: chr20:g.30407949A>G (hg19) chr20:g.31820146A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820146A>G , CM000682.2:g.31820146A>G GRCh38
NC_000020.10:g.30407949A>G , CM000682.1:g.30407949A>G GRCh37
NC_000020.9:g.29871610A>G NCBI36
NG_012847.1:g.5772A>G , LRG_392:g.5772A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.73A>G MANE Select ENSP00000365152.4:p.Thr25Ala
ENST00000375985.4:c.73A>G ENSP00000365152.4:p.Thr25Ala
ENST00000375994.6:c.73A>G ENSP00000365162.2:p.Thr25Ala
NM_033118.3:c.73A>G , LRG_392t1:c.73A>G NP_149109.1:p.Thr25Ala
XR_244155.1:n.238A>G
NM_033118.4:c.73A>G MANE Select NP_149109.1:p.Thr25Ala
Search 100 bp 5'
Search 100 bp 3'