Canonical Allele Identifier: CA2700692414
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs2105572487
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845685T>C , CM000664.2:g.135845685T>C GRCh38
NC_000002.11:g.136603255T>C , CM000664.1:g.136603255T>C GRCh37
NC_000002.10:g.136319725T>C NCBI36
NG_008104.2:g.14485A>G , LRG_338:g.14485A>G
NG_008958.1:g.35757A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+552A>G MANE Select ENSP00000264156.2:n.2209+552A>G
ENST00000264156.2:c.2209+552A>G ENSP00000264156.2:n.2209+552A>G
ENST00000492091.1:n.635+552A>G
NM_005915.5:c.2209+552A>G NP_005906.2:n.2209+552A>G
NM_005915.6:c.2209+552A>G MANE Select NP_005906.2:n.2209+552A>G
Search 100 bp 5'
Search 100 bp 3'