Canonical Allele Identifier: CA1290852260
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1679895445

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856541del , CM000664.2:g.135856541del GRCh38
NC_000002.11:g.136614111del , CM000664.1:g.136614111del GRCh37
NC_000002.10:g.136330581del NCBI36
NG_008104.2:g.3629del , LRG_338:g.3629del
NG_008958.1:g.24901del

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+187del MANE Select ENSP00000264156.2:n.1626+187del
ENST00000264156.2:c.1626+187del ENSP00000264156.2:n.1626+187del
ENST00000492091.1:n.182-4978del
NM_005915.5:c.1626+187del NP_005906.2:n.1626+187del
NM_005915.6:c.1626+187del MANE Select NP_005906.2:n.1626+187del