Canonical Allele Identifier: CA1290852244
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1679895021

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856501del , CM000664.2:g.135856501del GRCh38
NC_000002.11:g.136614071del , CM000664.1:g.136614071del GRCh37
NC_000002.10:g.136330541del NCBI36
NG_008104.2:g.3669del , LRG_338:g.3669del
NG_008958.1:g.24941del

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+227del MANE Select ENSP00000264156.2:n.1626+227del
ENST00000264156.2:c.1626+227del ENSP00000264156.2:n.1626+227del
ENST00000492091.1:n.182-4938del
NM_005915.5:c.1626+227del NP_005906.2:n.1626+227del
NM_005915.6:c.1626+227del MANE Select NP_005906.2:n.1626+227del