Canonical Allele Identifier: CA348659203

Gene: CXCR4

Linked Data

• dbSNP Id: rs1336721760
• gnomAD v2: 2-136873094-T-C
• gnomAD v4: 2-136115524-T-C
• MyVariant Identifiers: chr2:g.136873094T>C (hg19) ; chr2:g.136115524T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115524T>C , CM000664.2:g.136115524T>C	GRCh38
NC_000002.11:g.136873094T>C , CM000664.1:g.136873094T>C	GRCh37
NC_000002.10:g.136589564T>C	NCBI36
NG_011587.1:g.7632A>G , LRG_51:g.7632A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.392A>G	ENSP00000512428.1:p.Tyr131Cys
ENST00000696137.1:c.359A>G	ENSP00000512429.1:p.Tyr120Cys
ENST00000696152.1:c.359A>G	ENSP00000512443.1:p.Tyr120Cys
ENST00000696228.1:c.392A>G	ENSP00000512494.1:p.Tyr131Cys
ENST00000241393.4:c.404A>G MANE Select	ENSP00000241393.3:p.Tyr135Cys
ENST00000241393.3:c.404A>G	ENSP00000241393.3:p.Tyr135Cys
ENST00000409817.1:c.416A>G	ENSP00000386884.1:p.Tyr139Cys
ENST00000466288.1:n.598A>G
NM_001008540.1:c.416A>G	NP_001008540.1:p.Tyr139Cys
NM_003467.2:c.404A>G , LRG_51t1:c.404A>G	NP_003458.1:p.Tyr135Cys
NM_001008540.2:c.416A>G	NP_001008540.1:p.Tyr139Cys
NM_001348056.1:c.617A>G	NP_001334985.1:p.Tyr206Cys
NM_001348059.1:c.503A>G	NP_001334988.1:p.Tyr168Cys
NM_001348060.1:c.359A>G	NP_001334989.1:p.Tyr120Cys
NM_001348056.2:c.617A>G	NP_001334985.1:p.Tyr206Cys
NM_001348059.2:c.503A>G	NP_001334988.1:p.Tyr168Cys
NM_001348060.2:c.359A>G	NP_001334989.1:p.Tyr120Cys
NM_003467.3:c.404A>G MANE Select	NP_003458.1:p.Tyr135Cys