Canonical Allele Identifier: CA1290853453
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859223A= , CM000664.2:g.135859223A= GRCh38
NC_000002.11:g.136616793A= , CM000664.1:g.136616793A= GRCh37
NC_000002.10:g.136333263A= NCBI36
NG_008104.2:g.947T= , LRG_338:g.947T=
NG_008958.1:g.22219T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+78T= MANE Select ENSP00000264156.2:n.1362+78T=
ENST00000264156.2:c.1362+78T= ENSP00000264156.2:n.1362+78T=
ENST00000492091.1:n.181+3384T=
NM_005915.5:c.1362+78T= NP_005906.2:n.1362+78T=
NM_005915.6:c.1362+78T= MANE Select NP_005906.2:n.1362+78T=
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