Canonical Allele Identifier: CA2752322157
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859211G>C , CM000664.2:g.135859211G>C GRCh38
NC_000002.11:g.136616781G>C , CM000664.1:g.136616781G>C GRCh37
NC_000002.10:g.136333251G>C NCBI36
NG_008104.2:g.959C>G , LRG_338:g.959C>G
NG_008958.1:g.22231C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+90C>G MANE Select ENSP00000264156.2:n.1362+90C>G
ENST00000264156.2:c.1362+90C>G ENSP00000264156.2:n.1362+90C>G
ENST00000492091.1:n.181+3396C>G
NM_005915.5:c.1362+90C>G NP_005906.2:n.1362+90C>G
NM_005915.6:c.1362+90C>G MANE Select NP_005906.2:n.1362+90C>G