Canonical Allele Identifier: CA2661278018
Gene: MCM6 HGNC NCBI

Linked Data

gnomAD v4: 2-135851261-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851261G>A , CM000664.2:g.135851261G>A GRCh38
NC_000002.11:g.136608831G>A , CM000664.1:g.136608831G>A GRCh37
NC_000002.10:g.136325301G>A NCBI36
NG_008104.2:g.8909C>T , LRG_338:g.8909C>T
NG_008958.1:g.30181C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1917+141C>T MANE Select ENSP00000264156.2:n.1917+141C>T
ENST00000264156.2:c.1917+141C>T ENSP00000264156.2:n.1917+141C>T
ENST00000483902.1:n.544+141C>T
ENST00000492091.1:n.343+141C>T
NM_005915.5:c.1917+141C>T NP_005906.2:n.1917+141C>T
NM_005915.6:c.1917+141C>T MANE Select NP_005906.2:n.1917+141C>T
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