Canonical Allele Identifier: CA1290852257
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856535A= , CM000664.2:g.135856535A= GRCh38
NC_000002.11:g.136614105A= , CM000664.1:g.136614105A= GRCh37
NC_000002.10:g.136330575A= NCBI36
NG_008104.2:g.3635T= , LRG_338:g.3635T=
NG_008958.1:g.24907T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626+193T= MANE Select ENSP00000264156.2:n.1626+193T=
ENST00000264156.2:c.1626+193T= ENSP00000264156.2:n.1626+193T=
ENST00000492091.1:n.182-4972T=
NM_005915.5:c.1626+193T= NP_005906.2:n.1626+193T=
NM_005915.6:c.1626+193T= MANE Select NP_005906.2:n.1626+193T=