Canonical Allele Identifier: CA1290849643
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135850966C= , CM000664.2:g.135850966C= GRCh38
NC_000002.11:g.136608536C= , CM000664.1:g.136608536C= GRCh37
NC_000002.10:g.136325006C= NCBI36
NG_008104.2:g.9204G= , LRG_338:g.9204G=
NG_008958.1:g.30476G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1917+436G= MANE Select ENSP00000264156.2:n.1917+436G=
ENST00000264156.2:c.1917+436G= ENSP00000264156.2:n.1917+436G=
ENST00000483902.1:n.544+436G=
ENST00000492091.1:n.343+436G=
NM_005915.5:c.1917+436G= NP_005906.2:n.1917+436G=
NM_005915.6:c.1917+436G= MANE Select NP_005906.2:n.1917+436G=