Canonical Allele Identifier: CA56601619

Gene: MCM6

Linked Data

• dbSNP Id: rs867648873
• MyVariant Identifiers: chr2:g.136608556T>C (hg19) ; chr2:g.135850986T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135850986T>C , CM000664.2:g.135850986T>C	GRCh38
NC_000002.11:g.136608556T>C , CM000664.1:g.136608556T>C	GRCh37
NC_000002.10:g.136325026T>C	NCBI36
NG_008104.2:g.9184A>G , LRG_338:g.9184A>G
NG_008958.1:g.30456A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264156.3:c.1917+416A>G MANE Select	ENSP00000264156.2:n.1917+416A>G
ENST00000264156.2:c.1917+416A>G	ENSP00000264156.2:n.1917+416A>G
ENST00000483902.1:n.544+416A>G
ENST00000492091.1:n.343+416A>G
NM_005915.5:c.1917+416A>G	NP_005906.2:n.1917+416A>G
NM_005915.6:c.1917+416A>G MANE Select	NP_005906.2:n.1917+416A>G