Canonical Allele Identifier: CA1290853452
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859215T= , CM000664.2:g.135859215T= GRCh38
NC_000002.11:g.136616785T= , CM000664.1:g.136616785T= GRCh37
NC_000002.10:g.136333255T= NCBI36
NG_008104.2:g.955A= , LRG_338:g.955A=
NG_008958.1:g.22227A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1362+86A= MANE Select ENSP00000264156.2:n.1362+86A=
ENST00000264156.2:c.1362+86A= ENSP00000264156.2:n.1362+86A=
ENST00000492091.1:n.181+3392A=
NM_005915.5:c.1362+86A= NP_005906.2:n.1362+86A=
NM_005915.6:c.1362+86A= MANE Select NP_005906.2:n.1362+86A=
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