Canonical Allele Identifier: CA9763660
Gene: MKKS HGNC NCBI

Linked Data

dbSNP Id: rs770463812

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412959T>C , CM000682.2:g.10412959T>C GRCh38
NC_000020.10:g.10393607T>C , CM000682.1:g.10393607T>C GRCh37
NC_000020.9:g.10341607T>C NCBI36
NG_009109.1:g.26260A>G
NG_009109.2:g.26260A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.556A>G ENSP00000498849.1:p.Ile186Val
ENST00000652676.1:n.459-259A>G
ENST00000347364.7:c.556A>G MANE Select ENSP00000246062.4:p.Ile186Val
ENST00000399054.6:c.556A>G ENSP00000382008.2:p.Ile186Val
NM_018848.3:c.556A>G NP_061336.1:p.Ile186Val
NM_170784.2:c.556A>G NP_740754.1:p.Ile186Val
NR_072977.1:n.364-4156A>G
NR_072977.2:n.347-4156A>G
NM_170784.3:c.556A>G MANE Select NP_740754.1:p.Ile186Val