Canonical Allele Identifier: CA348594668
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856728C>A , CM000664.2:g.135856728C>A GRCh38
NC_000002.11:g.136614298C>A , CM000664.1:g.136614298C>A GRCh37
NC_000002.10:g.136330768C>A NCBI36
NG_008104.2:g.3442G>T , LRG_338:g.3442G>T
NG_008958.1:g.24714G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626G>T MANE Select ENSP00000264156.2:p.Glu542Asp
ENST00000264156.2:c.1626G>T ENSP00000264156.2:p.Glu542Asp
ENST00000492091.1:n.182-5165G>T
NM_005915.5:c.1626G>T NP_005906.2:p.Glu542Asp
NM_005915.6:c.1626G>T MANE Select NP_005906.2:p.Glu542Asp