Canonical Allele Identifier: CA1290847318
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845680A= , CM000664.2:g.135845680A= GRCh38
NC_000002.11:g.136603250A= , CM000664.1:g.136603250A= GRCh37
NC_000002.10:g.136319720A= NCBI36
NG_008104.2:g.14490T= , LRG_338:g.14490T=
NG_008958.1:g.35762T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+557T= MANE Select ENSP00000264156.2:n.2209+557T=
ENST00000264156.2:c.2209+557T= ENSP00000264156.2:n.2209+557T=
ENST00000492091.1:n.635+557T=
NM_005915.5:c.2209+557T= NP_005906.2:n.2209+557T=
NM_005915.6:c.2209+557T= MANE Select NP_005906.2:n.2209+557T=
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