Canonical Allele Identifier: CA401339500
Gene: CBX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.79784681A>T , CM000679.2:g.79784681A>T GRCh38
NC_000017.10:g.77758480A>T , CM000679.1:g.77758480A>T GRCh37
NC_000017.9:g.75373075A>T NCBI36
NG_016986.1:g.11504A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310942.9:c.1238A>T MANE Select ENSP00000308750.4:p.Lys413Met
ENST00000310942.8:c.1238A>T ENSP00000308750.4:p.Lys413Met
NM_005189.2:c.1238A>T NP_005180.1:p.Lys413Met
XM_011525382.1:c.1238A>T XP_011523684.1:p.Lys413Met
XM_011525383.1:c.983A>T XP_011523685.1:p.Lys328Met
XM_011525383.2:c.983A>T XP_011523685.1:p.Lys328Met
NM_005189.3:c.1238A>T MANE Select NP_005180.1:p.Lys413Met