Canonical Allele Identifier: CA536398730
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1407665614
gnomAD v2: 2-136603261-T-G
gnomAD v3: 2-135845691-T-G
gnomAD v4: 2-135845691-T-G
MyVariant Identifiers: chr2:g.136603261T>G (hg19) chr2:g.135845691T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135845691T>G , CM000664.2:g.135845691T>G GRCh38
NC_000002.11:g.136603261T>G , CM000664.1:g.136603261T>G GRCh37
NC_000002.10:g.136319731T>G NCBI36
NG_008104.2:g.14479A>C , LRG_338:g.14479A>C
NG_008958.1:g.35751A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.2209+546A>C MANE Select ENSP00000264156.2:n.2209+546A>C
ENST00000264156.2:c.2209+546A>C ENSP00000264156.2:n.2209+546A>C
ENST00000492091.1:n.635+546A>C
NM_005915.5:c.2209+546A>C NP_005906.2:n.2209+546A>C
NM_005915.6:c.2209+546A>C MANE Select NP_005906.2:n.2209+546A>C
Search 100 bp 5'
Search 100 bp 3'