Canonical Allele Identifier: CA2661278689
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v4: 2-135859161-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859164del , CM000664.2:g.135859164del GRCh38
NC_000002.11:g.136616734del , CM000664.1:g.136616734del GRCh37
NC_000002.10:g.136333204del NCBI36
NG_008104.2:g.1008del , LRG_338:g.1008del
NG_008958.1:g.22280del

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1362+139del MANE Select ENSP00000264156.2:n.1362+139del
ENST00000264156.2:c.1362+139del ENSP00000264156.2:n.1362+139del
ENST00000492091.1:n.181+3445del
NM_005915.5:c.1362+139del NP_005906.2:n.1362+139del
NM_005915.6:c.1362+139del MANE Select NP_005906.2:n.1362+139del
Search 100 bp 5'
Search 100 bp 3'