Canonical Allele Identifier: CA2652342966
Gene: MYLK2 HGNC NCBI

Linked Data

gnomAD v4: 20-31820070-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31820070G>C , CM000682.2:g.31820070G>C GRCh38
NC_000020.10:g.30407873G>C , CM000682.1:g.30407873G>C GRCh37
NC_000020.9:g.29871534G>C NCBI36
NG_012847.1:g.5696G>C , LRG_392:g.5696G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53-56G>C MANE Select ENSP00000365152.4:n.53-56G>C
ENST00000375985.4:c.53-56G>C ENSP00000365152.4:n.53-56G>C
ENST00000375994.6:c.53-56G>C ENSP00000365162.2:n.53-56G>C
NM_033118.3:c.53-56G>C , LRG_392t1:c.53-56G>C NP_149109.1:n.53-56G>C
XR_244155.1:n.218-56G>C
NM_033118.4:c.53-56G>C MANE Select NP_149109.1:n.53-56G>C
Search 100 bp 5'
Search 100 bp 3'