Canonical Allele Identifier: CA1290849732
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851168G= , CM000664.2:g.135851168G= GRCh38
NC_000002.11:g.136608738G= , CM000664.1:g.136608738G= GRCh37
NC_000002.10:g.136325208G= NCBI36
NG_008104.2:g.9002C= , LRG_338:g.9002C=
NG_008958.1:g.30274C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1917+234C= MANE Select ENSP00000264156.2:n.1917+234C=
ENST00000264156.2:c.1917+234C= ENSP00000264156.2:n.1917+234C=
ENST00000483902.1:n.544+234C=
ENST00000492091.1:n.343+234C=
NM_005915.5:c.1917+234C= NP_005906.2:n.1917+234C=
NM_005915.6:c.1917+234C= MANE Select NP_005906.2:n.1917+234C=
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