Canonical Allele Identifier: CA2661278834
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v4: 2-135856613-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856613A>G , CM000664.2:g.135856613A>G GRCh38
NC_000002.11:g.136614183A>G , CM000664.1:g.136614183A>G GRCh37
NC_000002.10:g.136330653A>G NCBI36
NG_008104.2:g.3557T>C , LRG_338:g.3557T>C
NG_008958.1:g.24829T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+115T>C MANE Select ENSP00000264156.2:n.1626+115T>C
ENST00000264156.2:c.1626+115T>C ENSP00000264156.2:n.1626+115T>C
ENST00000492091.1:n.182-5050T>C
NM_005915.5:c.1626+115T>C NP_005906.2:n.1626+115T>C
NM_005915.6:c.1626+115T>C MANE Select NP_005906.2:n.1626+115T>C
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