Canonical Allele Identifier: CA502399582
Gene: CBX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.77758478G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.79784679G>A , CM000679.2:g.79784679G>A GRCh38
NC_000017.10:g.77758478G>A , CM000679.1:g.77758478G>A GRCh37
NC_000017.9:g.75373073G>A NCBI36
NG_016986.1:g.11502G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310942.9:c.1236G>A MANE Select ENSP00000308750.4:p.Glu412=
ENST00000310942.8:c.1236G>A ENSP00000308750.4:p.Glu412=
NM_005189.2:c.1236G>A NP_005180.1:p.Glu412=
XM_011525382.1:c.1236G>A XP_011523684.1:p.Glu412=
XM_011525383.1:c.981G>A XP_011523685.1:p.Glu327=
XM_011525383.2:c.981G>A XP_011523685.1:p.Glu327=
NM_005189.3:c.1236G>A MANE Select NP_005180.1:p.Glu412=