Canonical Allele Identifier: CA1290849725
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851139C= , CM000664.2:g.135851139C= GRCh38
NC_000002.11:g.136608709C= , CM000664.1:g.136608709C= GRCh37
NC_000002.10:g.136325179C= NCBI36
NG_008104.2:g.9031G= , LRG_338:g.9031G=
NG_008958.1:g.30303G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+263G= MANE Select ENSP00000264156.2:n.1917+263G=
ENST00000264156.2:c.1917+263G= ENSP00000264156.2:n.1917+263G=
ENST00000483902.1:n.544+263G=
ENST00000492091.1:n.343+263G=
NM_005915.5:c.1917+263G= NP_005906.2:n.1917+263G=
NM_005915.6:c.1917+263G= MANE Select NP_005906.2:n.1917+263G=
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