Canonical Allele Identifier: CA1036808333
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1679657472
gnomAD v3: 2-135845666-A-T
gnomAD v4: 2-135845666-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845666A>T , CM000664.2:g.135845666A>T GRCh38
NC_000002.11:g.136603236A>T , CM000664.1:g.136603236A>T GRCh37
NC_000002.10:g.136319706A>T NCBI36
NG_008104.2:g.14504T>A , LRG_338:g.14504T>A
NG_008958.1:g.35776T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+571T>A MANE Select ENSP00000264156.2:n.2209+571T>A
ENST00000264156.2:c.2209+571T>A ENSP00000264156.2:n.2209+571T>A
ENST00000492091.1:n.635+571T>A
NM_005915.5:c.2209+571T>A NP_005906.2:n.2209+571T>A
NM_005915.6:c.2209+571T>A MANE Select NP_005906.2:n.2209+571T>A
Search 100 bp 5'
Search 100 bp 3'