Canonical Allele Identifier: CA2577118748
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856709del , CM000664.2:g.135856709del GRCh38
NC_000002.11:g.136614279del , CM000664.1:g.136614279del GRCh37
NC_000002.10:g.136330749del NCBI36
NG_008104.2:g.3466del , LRG_338:g.3466del
NG_008958.1:g.24738del

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+24del MANE Select ENSP00000264156.2:n.1626+24del
ENST00000264156.2:c.1626+24del ENSP00000264156.2:n.1626+24del
ENST00000492091.1:n.182-5141del
NM_005915.5:c.1626+24del NP_005906.2:n.1626+24del
NM_005915.6:c.1626+24del MANE Select NP_005906.2:n.1626+24del