Canonical Allele Identifier: CA452026190

Gene: MCM9

Linked Data

• MyVariant Identifiers: chr6:g.119149100T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118827937T>C , CM000668.2:g.118827937T>C	GRCh38
NC_000006.11:g.119149100T>C , CM000668.1:g.119149100T>C	GRCh37
NC_000006.10:g.119255792T>C	NCBI36
NG_041822.1:g.112226A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619706.5:c.1722A>G MANE Select	ENSP00000480469.1:p.Arg574=
ENST00000316316.10:c.1722A>G	ENSP00000314505.5:p.Arg574=
ENST00000458674.2:c.207-1073A>G
ENST00000619706.4:c.1722A>G	ENSP00000480469.1:p.Arg574=
NM_017696.2:c.1722A>G	NP_060166.2:p.Arg574=
NM_001378356.1:c.1722A>G	NP_001365285.1:p.Arg574=
NM_001378357.1:c.1722A>G	NP_001365286.1:p.Arg574=
NM_001378359.1:c.1722A>G	NP_001365288.1:p.Arg574=
NM_001378360.1:c.1722A>G	NP_001365289.1:p.Arg574=
NM_001378364.1:c.1529-1073A>G	NP_001365293.1:n.1529-1073A>G
NM_001378366.1:c.1596A>G	NP_001365295.1:p.Arg532=
NM_001378367.1:c.1524A>G	NP_001365296.1:p.Arg508=
NM_017696.3:c.1722A>G MANE Select	NP_060166.2:p.Arg574=
NR_165493.1:n.1831A>G