Canonical Allele Identifier: CA2838009331
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851194A>C , CM000664.2:g.135851194A>C GRCh38
NC_000002.11:g.136608764A>C , CM000664.1:g.136608764A>C GRCh37
NC_000002.10:g.136325234A>C NCBI36
NG_008104.2:g.8976T>G , LRG_338:g.8976T>G
NG_008958.1:g.30248T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1917+208T>G MANE Select ENSP00000264156.2:n.1917+208T>G
ENST00000264156.2:c.1917+208T>G ENSP00000264156.2:n.1917+208T>G
ENST00000483902.1:n.544+208T>G
ENST00000492091.1:n.343+208T>G
NM_005915.5:c.1917+208T>G NP_005906.2:n.1917+208T>G
NM_005915.6:c.1917+208T>G MANE Select NP_005906.2:n.1917+208T>G