Canonical Allele Identifier: CA1290849781
Gene: MCM6 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851251T= , CM000664.2:g.135851251T= GRCh38
NC_000002.11:g.136608821T= , CM000664.1:g.136608821T= GRCh37
NC_000002.10:g.136325291T= NCBI36
NG_008104.2:g.8919A= , LRG_338:g.8919A=
NG_008958.1:g.30191A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+151A= MANE Select ENSP00000264156.2:n.1917+151A=
ENST00000264156.2:c.1917+151A= ENSP00000264156.2:n.1917+151A=
ENST00000483902.1:n.544+151A=
ENST00000492091.1:n.343+151A=
NM_005915.5:c.1917+151A= NP_005906.2:n.1917+151A=
NM_005915.6:c.1917+151A= MANE Select NP_005906.2:n.1917+151A=
Search 100 bp 5'
Search 100 bp 3'