Canonical Allele Identifier: CA1290852357
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856732T= , CM000664.2:g.135856732T= GRCh38
NC_000002.11:g.136614302T= , CM000664.1:g.136614302T= GRCh37
NC_000002.10:g.136330772T= NCBI36
NG_008104.2:g.3438A= , LRG_338:g.3438A=
NG_008958.1:g.24710A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1622A= MANE Select ENSP00000264156.2:p.Asn541=
ENST00000264156.2:c.1622A= ENSP00000264156.2:p.Asn541=
ENST00000492091.1:n.182-5169A=
NM_005915.5:c.1622A= NP_005906.2:p.Asn541=
NM_005915.6:c.1622A= MANE Select NP_005906.2:p.Asn541=