Canonical Allele Identifier: CA1290852310
Gene: MCM6 HGNC NCBI

Linked Data

dbSNP Id: rs1679896722
gnomAD v4: 2-135856621-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856621C>A , CM000664.2:g.135856621C>A GRCh38
NC_000002.11:g.136614191C>A , CM000664.1:g.136614191C>A GRCh37
NC_000002.10:g.136330661C>A NCBI36
NG_008104.2:g.3549G>T , LRG_338:g.3549G>T
NG_008958.1:g.24821G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+107G>T MANE Select ENSP00000264156.2:n.1626+107G>T
ENST00000264156.2:c.1626+107G>T ENSP00000264156.2:n.1626+107G>T
ENST00000492091.1:n.182-5058G>T
NM_005915.5:c.1626+107G>T NP_005906.2:n.1626+107G>T
NM_005915.6:c.1626+107G>T MANE Select NP_005906.2:n.1626+107G>T
Search 100 bp 5'
Search 100 bp 3'