Canonical Allele Identifier: CA2661278767
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856585del , CM000664.2:g.135856585del GRCh38
NC_000002.11:g.136614155del , CM000664.1:g.136614155del GRCh37
NC_000002.10:g.136330625del NCBI36
NG_008104.2:g.3587del , LRG_338:g.3587del
NG_008958.1:g.24859del

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+145del MANE Select ENSP00000264156.2:n.1626+145del
ENST00000264156.2:c.1626+145del ENSP00000264156.2:n.1626+145del
ENST00000492091.1:n.182-5020del
NM_005915.5:c.1626+145del NP_005906.2:n.1626+145del
NM_005915.6:c.1626+145del MANE Select NP_005906.2:n.1626+145del