Canonical Allele Identifier: CA1036808339
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v3: 2-135845692-G-T
gnomAD v4: 2-135845692-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845692G>T , CM000664.2:g.135845692G>T GRCh38
NC_000002.11:g.136603262G>T , CM000664.1:g.136603262G>T GRCh37
NC_000002.10:g.136319732G>T NCBI36
NG_008104.2:g.14478C>A , LRG_338:g.14478C>A
NG_008958.1:g.35750C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+545C>A MANE Select ENSP00000264156.2:n.2209+545C>A
ENST00000264156.2:c.2209+545C>A ENSP00000264156.2:n.2209+545C>A
ENST00000492091.1:n.635+545C>A
NM_005915.5:c.2209+545C>A NP_005906.2:n.2209+545C>A
NM_005915.6:c.2209+545C>A MANE Select NP_005906.2:n.2209+545C>A
Search 100 bp 5'
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