Canonical Allele Identifier: CA2661278814
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v4: 2-135856604-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856604G>T , CM000664.2:g.135856604G>T GRCh38
NC_000002.11:g.136614174G>T , CM000664.1:g.136614174G>T GRCh37
NC_000002.10:g.136330644G>T NCBI36
NG_008104.2:g.3566C>A , LRG_338:g.3566C>A
NG_008958.1:g.24838C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+124C>A MANE Select ENSP00000264156.2:n.1626+124C>A
ENST00000264156.2:c.1626+124C>A ENSP00000264156.2:n.1626+124C>A
ENST00000492091.1:n.182-5041C>A
NM_005915.5:c.1626+124C>A NP_005906.2:n.1626+124C>A
NM_005915.6:c.1626+124C>A MANE Select NP_005906.2:n.1626+124C>A
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