Canonical Allele Identifier: CA429085905
Gene: MCM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.136614298C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856728C>T , CM000664.2:g.135856728C>T GRCh38
NC_000002.11:g.136614298C>T , CM000664.1:g.136614298C>T GRCh37
NC_000002.10:g.136330768C>T NCBI36
NG_008104.2:g.3442G>A , LRG_338:g.3442G>A
NG_008958.1:g.24714G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626G>A MANE Select ENSP00000264156.2:p.Glu542=
ENST00000264156.2:c.1626G>A ENSP00000264156.2:p.Glu542=
ENST00000492091.1:n.182-5165G>A
NM_005915.5:c.1626G>A NP_005906.2:p.Glu542=
NM_005915.6:c.1626G>A MANE Select NP_005906.2:p.Glu542=
Search 100 bp 5'
Search 100 bp 3'