Canonical Allele Identifier: CA502399589
Gene: CBX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.77758484G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.79784685G>C , CM000679.2:g.79784685G>C GRCh38
NC_000017.10:g.77758484G>C , CM000679.1:g.77758484G>C GRCh37
NC_000017.9:g.75373079G>C NCBI36
NG_016986.1:g.11508G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000310942.9:c.1242G>C MANE Select ENSP00000308750.4:p.Leu414=
ENST00000310942.8:c.1242G>C ENSP00000308750.4:p.Leu414=
NM_005189.2:c.1242G>C NP_005180.1:p.Leu414=
XM_011525382.1:c.1242G>C XP_011523684.1:p.Leu414=
XM_011525383.1:c.987G>C XP_011523685.1:p.Leu329=
XM_011525383.2:c.987G>C XP_011523685.1:p.Leu329=
NM_005189.3:c.1242G>C MANE Select NP_005180.1:p.Leu414=
Search 100 bp 5'
Search 100 bp 3'