Canonical Allele Identifier: CA1016909100
Gene: MYLK2 HGNC NCBI

Linked Data

dbSNP Id: rs2062266552
gnomAD v3: 20-31824185-G-C
gnomAD v4: 20-31824185-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824185G>C , CM000682.2:g.31824185G>C GRCh38
NC_000020.10:g.30411988G>C , CM000682.1:g.30411988G>C GRCh37
NC_000020.9:g.29875649G>C NCBI36
NG_012847.1:g.9811G>C , LRG_392:g.9811G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.879-74G>C MANE Select ENSP00000365152.4:n.879-74G>C
ENST00000375985.4:c.879-74G>C ENSP00000365152.4:n.879-74G>C
ENST00000375994.6:c.879-74G>C ENSP00000365162.2:n.879-74G>C
NM_033118.3:c.879-74G>C , LRG_392t1:c.879-74G>C NP_149109.1:n.879-74G>C
XR_244155.1:n.1244+62G>C
NM_033118.4:c.879-74G>C MANE Select NP_149109.1:n.879-74G>C
Search 100 bp 5'
Search 100 bp 3'