Canonical Allele Identifier: CA1016907500
Gene: MYLK2 HGNC NCBI

Linked Data

dbSNP Id: rs2062243734
gnomAD v3: 20-31820095-G-A
gnomAD v4: 20-31820095-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820095G>A , CM000682.2:g.31820095G>A GRCh38
NC_000020.10:g.30407898G>A , CM000682.1:g.30407898G>A GRCh37
NC_000020.9:g.29871559G>A NCBI36
NG_012847.1:g.5721G>A , LRG_392:g.5721G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53-31G>A MANE Select ENSP00000365152.4:n.53-31G>A
ENST00000375985.4:c.53-31G>A ENSP00000365152.4:n.53-31G>A
ENST00000375994.6:c.53-31G>A ENSP00000365162.2:n.53-31G>A
NM_033118.3:c.53-31G>A , LRG_392t1:c.53-31G>A NP_149109.1:n.53-31G>A
XR_244155.1:n.218-31G>A
NM_033118.4:c.53-31G>A MANE Select NP_149109.1:n.53-31G>A
Search 100 bp 5'
Search 100 bp 3'