Canonical Allele Identifier: CA56601900
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs868107896
MyVariant Identifiers: chr2:g.136608766A>G (hg19) chr2:g.135851196A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851196A>G , CM000664.2:g.135851196A>G GRCh38
NC_000002.11:g.136608766A>G , CM000664.1:g.136608766A>G GRCh37
NC_000002.10:g.136325236A>G NCBI36
NG_008104.2:g.8974T>C , LRG_338:g.8974T>C
NG_008958.1:g.30246T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+206T>C MANE Select ENSP00000264156.2:n.1917+206T>C
ENST00000264156.2:c.1917+206T>C ENSP00000264156.2:n.1917+206T>C
ENST00000483902.1:n.544+206T>C
ENST00000492091.1:n.343+206T>C
NM_005915.5:c.1917+206T>C NP_005906.2:n.1917+206T>C
NM_005915.6:c.1917+206T>C MANE Select NP_005906.2:n.1917+206T>C
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