Canonical Allele Identifier: CA2661278654
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859152C>A , CM000664.2:g.135859152C>A GRCh38
NC_000002.11:g.136616722C>A , CM000664.1:g.136616722C>A GRCh37
NC_000002.10:g.136333192C>A NCBI36
NG_008104.2:g.1018G>T , LRG_338:g.1018G>T
NG_008958.1:g.22290G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1362+149G>T MANE Select ENSP00000264156.2:n.1362+149G>T
ENST00000264156.2:c.1362+149G>T ENSP00000264156.2:n.1362+149G>T
ENST00000492091.1:n.181+3455G>T
NM_005915.5:c.1362+149G>T NP_005906.2:n.1362+149G>T
NM_005915.6:c.1362+149G>T MANE Select NP_005906.2:n.1362+149G>T