Canonical Allele Identifier: CA1290853390
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859064T= , CM000664.2:g.135859064T= GRCh38
NC_000002.11:g.136616634T= , CM000664.1:g.136616634T= GRCh37
NC_000002.10:g.136333104T= NCBI36
NG_008104.2:g.1106A= , LRG_338:g.1106A=
NG_008958.1:g.22378A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1362+237A= MANE Select ENSP00000264156.2:n.1362+237A=
ENST00000264156.2:c.1362+237A= ENSP00000264156.2:n.1362+237A=
ENST00000492091.1:n.181+3543A=
NM_005915.5:c.1362+237A= NP_005906.2:n.1362+237A=
NM_005915.6:c.1362+237A= MANE Select NP_005906.2:n.1362+237A=
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