Canonical Allele Identifier: CA365550929

Gene: MCM9

Linked Data

• MyVariant Identifiers: chr6:g.119149102G>C (hg19) ; chr6:g.118827939G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827939G>C , CM000668.2:g.118827939G>C	GRCh38
NC_000006.11:g.119149102G>C , CM000668.1:g.119149102G>C	GRCh37
NC_000006.10:g.119255794G>C	NCBI36
NG_041822.1:g.112224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1720C>G MANE Select	ENSP00000480469.1:p.Arg574Gly
ENST00000316316.10:c.1720C>G	ENSP00000314505.5:p.Arg574Gly
ENST00000458674.2:c.207-1075C>G
ENST00000619706.4:c.1720C>G	ENSP00000480469.1:p.Arg574Gly
NM_017696.2:c.1720C>G	NP_060166.2:p.Arg574Gly
NM_001378356.1:c.1720C>G	NP_001365285.1:p.Arg574Gly
NM_001378357.1:c.1720C>G	NP_001365286.1:p.Arg574Gly
NM_001378359.1:c.1720C>G	NP_001365288.1:p.Arg574Gly
NM_001378360.1:c.1720C>G	NP_001365289.1:p.Arg574Gly
NM_001378364.1:c.1529-1075C>G	NP_001365293.1:n.1529-1075C>G
NM_001378366.1:c.1594C>G	NP_001365295.1:p.Arg532Gly
NM_001378367.1:c.1522C>G	NP_001365296.1:p.Arg508Gly
NM_017696.3:c.1720C>G MANE Select	NP_060166.2:p.Arg574Gly
NR_165493.1:n.1829C>G