Canonical Allele Identifier: CA2752321703
Gene: MCM6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851013C>A , CM000664.2:g.135851013C>A GRCh38
NC_000002.11:g.136608583C>A , CM000664.1:g.136608583C>A GRCh37
NC_000002.10:g.136325053C>A NCBI36
NG_008104.2:g.9157G>T , LRG_338:g.9157G>T
NG_008958.1:g.30429G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+389G>T MANE Select ENSP00000264156.2:n.1917+389G>T
ENST00000264156.2:c.1917+389G>T ENSP00000264156.2:n.1917+389G>T
ENST00000483902.1:n.544+389G>T
ENST00000492091.1:n.343+389G>T
NM_005915.5:c.1917+389G>T NP_005906.2:n.1917+389G>T
NM_005915.6:c.1917+389G>T MANE Select NP_005906.2:n.1917+389G>T
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