Canonical Allele Identifier: CA502399585
Gene: CBX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.77758482C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.79784683C>T , CM000679.2:g.79784683C>T GRCh38
NC_000017.10:g.77758482C>T , CM000679.1:g.77758482C>T GRCh37
NC_000017.9:g.75373077C>T NCBI36
NG_016986.1:g.11506C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310942.9:c.1240C>T MANE Select ENSP00000308750.4:p.Leu414=
ENST00000310942.8:c.1240C>T ENSP00000308750.4:p.Leu414=
NM_005189.2:c.1240C>T NP_005180.1:p.Leu414=
XM_011525382.1:c.1240C>T XP_011523684.1:p.Leu414=
XM_011525383.1:c.985C>T XP_011523685.1:p.Leu329=
XM_011525383.2:c.985C>T XP_011523685.1:p.Leu329=
NM_005189.3:c.1240C>T MANE Select NP_005180.1:p.Leu414=