Canonical Allele Identifier: CA2661278669
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v4: 2-135859158-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859158T>G , CM000664.2:g.135859158T>G GRCh38
NC_000002.11:g.136616728T>G , CM000664.1:g.136616728T>G GRCh37
NC_000002.10:g.136333198T>G NCBI36
NG_008104.2:g.1012A>C , LRG_338:g.1012A>C
NG_008958.1:g.22284A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1362+143A>C MANE Select ENSP00000264156.2:n.1362+143A>C
ENST00000264156.2:c.1362+143A>C ENSP00000264156.2:n.1362+143A>C
ENST00000492091.1:n.181+3449A>C
NM_005915.5:c.1362+143A>C NP_005906.2:n.1362+143A>C
NM_005915.6:c.1362+143A>C MANE Select NP_005906.2:n.1362+143A>C
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