Canonical Allele Identifier: CA348594670
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856729T>A , CM000664.2:g.135856729T>A GRCh38
NC_000002.11:g.136614299T>A , CM000664.1:g.136614299T>A GRCh37
NC_000002.10:g.136330769T>A NCBI36
NG_008104.2:g.3441A>T , LRG_338:g.3441A>T
NG_008958.1:g.24713A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1625A>T MANE Select ENSP00000264156.2:p.Glu542Val
ENST00000264156.2:c.1625A>T ENSP00000264156.2:p.Glu542Val
ENST00000492091.1:n.182-5166A>T
NM_005915.5:c.1625A>T NP_005906.2:p.Glu542Val
NM_005915.6:c.1625A>T MANE Select NP_005906.2:p.Glu542Val