Canonical Allele Identifier: CA123717
Gene: CXCR4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14023
ClinVar RCV Id: RCV000015067
dbSNP Id: rs104893626

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.136114915G>C , CM000664.2:g.136114915G>C GRCh38
NC_000002.11:g.136872485G>C , CM000664.1:g.136872485G>C GRCh37
NC_000002.10:g.136588955G>C NCBI36
NG_011587.1:g.8241C>G , LRG_51:g.8241C>G

Transcript Alleles

HGVS Amino-acid change
NM_001008540.1:c.1025C>G VV NP_001008540.1:p.Ser342Ter
NM_003467.2:c.1013C>G , LRG_51t1:c.1013C>G NP_003458.1:p.Ser338Ter
NM_001008540.2:c.1025C>G VV
NM_001348056.1:c.1226C>G VV NP_001334985.1:p.Ser409Ter
NM_001348059.1:c.1112C>G VV NP_001334988.1:p.Ser371Ter
NM_001348060.1:c.968C>G VV NP_001334989.1:p.Ser323Ter
ENST00000241393.3:c.1013C>G ENSP00000241393.3:p.Ser338Ter
ENST00000409817.1:c.1025C>G ENSP00000386884.1:p.Ser342Ter
ENST00000466288.1:n.1207C>G