Canonical Allele Identifier: CA2661278836
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v4: 2-135859209-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859209A>T , CM000664.2:g.135859209A>T GRCh38
NC_000002.11:g.136616779A>T , CM000664.1:g.136616779A>T GRCh37
NC_000002.10:g.136333249A>T NCBI36
NG_008104.2:g.961T>A , LRG_338:g.961T>A
NG_008958.1:g.22233T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+92T>A MANE Select ENSP00000264156.2:n.1362+92T>A
ENST00000264156.2:c.1362+92T>A ENSP00000264156.2:n.1362+92T>A
ENST00000492091.1:n.181+3398T>A
NM_005915.5:c.1362+92T>A NP_005906.2:n.1362+92T>A
NM_005915.6:c.1362+92T>A MANE Select NP_005906.2:n.1362+92T>A
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