Canonical Allele Identifier: CA401339402
Gene: CBX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.79784671A>T , CM000679.2:g.79784671A>T GRCh38
NC_000017.10:g.77758470A>T , CM000679.1:g.77758470A>T GRCh37
NC_000017.9:g.75373065A>T NCBI36
NG_016986.1:g.11494A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000310942.9:c.1228A>T MANE Select ENSP00000308750.4:p.Lys410Ter
ENST00000310942.8:c.1228A>T ENSP00000308750.4:p.Lys410Ter
NM_005189.2:c.1228A>T NP_005180.1:p.Lys410Ter
XM_011525382.1:c.1228A>T XP_011523684.1:p.Lys410Ter
XM_011525383.1:c.973A>T XP_011523685.1:p.Lys325Ter
XM_011525383.2:c.973A>T XP_011523685.1:p.Lys325Ter
NM_005189.3:c.1228A>T MANE Select NP_005180.1:p.Lys410Ter