Canonical Allele Identifier: CA1290853449
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859207T= , CM000664.2:g.135859207T= GRCh38
NC_000002.11:g.136616777T= , CM000664.1:g.136616777T= GRCh37
NC_000002.10:g.136333247T= NCBI36
NG_008104.2:g.963A= , LRG_338:g.963A=
NG_008958.1:g.22235A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+94A= MANE Select ENSP00000264156.2:n.1362+94A=
ENST00000264156.2:c.1362+94A= ENSP00000264156.2:n.1362+94A=
ENST00000492091.1:n.181+3400A=
NM_005915.5:c.1362+94A= NP_005906.2:n.1362+94A=
NM_005915.6:c.1362+94A= MANE Select NP_005906.2:n.1362+94A=
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