Canonical Allele Identifier: CA56601498
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs893578023
gnomAD v3: 2-135850918-C-T
gnomAD v4: 2-135850918-C-T
MyVariant Identifiers: chr2:g.136608488C>T (hg19) chr2:g.135850918C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135850918C>T , CM000664.2:g.135850918C>T GRCh38
NC_000002.11:g.136608488C>T , CM000664.1:g.136608488C>T GRCh37
NC_000002.10:g.136324958C>T NCBI36
NG_008104.2:g.9252G>A , LRG_338:g.9252G>A
NG_008958.1:g.30524G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1917+484G>A MANE Select ENSP00000264156.2:n.1917+484G>A
ENST00000264156.2:c.1917+484G>A ENSP00000264156.2:n.1917+484G>A
ENST00000483902.1:n.544+484G>A
ENST00000492091.1:n.343+484G>A
NM_005915.5:c.1917+484G>A NP_005906.2:n.1917+484G>A
NM_005915.6:c.1917+484G>A MANE Select NP_005906.2:n.1917+484G>A
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