Canonical Allele Identifier: CA348658687

Gene: CXCR4

Linked Data

• dbSNP Id: rs2104917251
• MyVariant Identifiers: chr2:g.136872986T>C (hg19) ; chr2:g.136115416T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115416T>C , CM000664.2:g.136115416T>C	GRCh38
NC_000002.11:g.136872986T>C , CM000664.1:g.136872986T>C	GRCh37
NC_000002.10:g.136589456T>C	NCBI36
NG_011587.1:g.7740A>G , LRG_51:g.7740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.500A>G	ENSP00000512428.1:p.Asp167Gly
ENST00000696137.1:c.467A>G	ENSP00000512429.1:p.Asp156Gly
ENST00000696152.1:c.467A>G	ENSP00000512443.1:p.Asp156Gly
ENST00000696228.1:c.500A>G	ENSP00000512494.1:p.Asp167Gly
ENST00000241393.4:c.512A>G MANE Select	ENSP00000241393.3:p.Asp171Gly
ENST00000241393.3:c.512A>G	ENSP00000241393.3:p.Asp171Gly
ENST00000409817.1:c.524A>G	ENSP00000386884.1:p.Asp175Gly
ENST00000466288.1:n.706A>G
NM_001008540.1:c.524A>G	NP_001008540.1:p.Asp175Gly
NM_003467.2:c.512A>G , LRG_51t1:c.512A>G	NP_003458.1:p.Asp171Gly
NM_001008540.2:c.524A>G	NP_001008540.1:p.Asp175Gly
NM_001348056.1:c.725A>G	NP_001334985.1:p.Asp242Gly
NM_001348059.1:c.611A>G	NP_001334988.1:p.Asp204Gly
NM_001348060.1:c.467A>G	NP_001334989.1:p.Asp156Gly
NM_001348056.2:c.725A>G	NP_001334985.1:p.Asp242Gly
NM_001348059.2:c.611A>G	NP_001334988.1:p.Asp204Gly
NM_001348060.2:c.467A>G	NP_001334989.1:p.Asp156Gly
NM_003467.3:c.512A>G MANE Select	NP_003458.1:p.Asp171Gly