Canonical Allele Identifier: CA2661278863
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859225G>A , CM000664.2:g.135859225G>A GRCh38
NC_000002.11:g.136616795G>A , CM000664.1:g.136616795G>A GRCh37
NC_000002.10:g.136333265G>A NCBI36
NG_008104.2:g.945C>T , LRG_338:g.945C>T
NG_008958.1:g.22217C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1362+76C>T MANE Select ENSP00000264156.2:n.1362+76C>T
ENST00000264156.2:c.1362+76C>T ENSP00000264156.2:n.1362+76C>T
ENST00000492091.1:n.181+3382C>T
NM_005915.5:c.1362+76C>T NP_005906.2:n.1362+76C>T
NM_005915.6:c.1362+76C>T MANE Select NP_005906.2:n.1362+76C>T