Canonical Allele Identifier: CA1290852313
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856630G= , CM000664.2:g.135856630G= GRCh38
NC_000002.11:g.136614200G= , CM000664.1:g.136614200G= GRCh37
NC_000002.10:g.136330670G= NCBI36
NG_008104.2:g.3540C= , LRG_338:g.3540C=
NG_008958.1:g.24812C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+98C= MANE Select ENSP00000264156.2:n.1626+98C=
ENST00000264156.2:c.1626+98C= ENSP00000264156.2:n.1626+98C=
ENST00000492091.1:n.182-5067C=
NM_005915.5:c.1626+98C= NP_005906.2:n.1626+98C=
NM_005915.6:c.1626+98C= MANE Select NP_005906.2:n.1626+98C=
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