Canonical Allele Identifier: CA1290847322
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845688T= , CM000664.2:g.135845688T= GRCh38
NC_000002.11:g.136603258T= , CM000664.1:g.136603258T= GRCh37
NC_000002.10:g.136319728T= NCBI36
NG_008104.2:g.14482A= , LRG_338:g.14482A=
NG_008958.1:g.35754A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+549A= MANE Select ENSP00000264156.2:n.2209+549A=
ENST00000264156.2:c.2209+549A= ENSP00000264156.2:n.2209+549A=
ENST00000492091.1:n.635+549A=
NM_005915.5:c.2209+549A= NP_005906.2:n.2209+549A=
NM_005915.6:c.2209+549A= MANE Select NP_005906.2:n.2209+549A=
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