Canonical Allele Identifier: CA429206643

Gene: CXCR4

Linked Data

• dbSNP Id: rs1684861118
• gnomAD v3: 2-136115529-G-A
• gnomAD v4: 2-136115529-G-A
• MyVariant Identifiers: chr2:g.136873099G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115529G>A , CM000664.2:g.136115529G>A	GRCh38
NC_000002.11:g.136873099G>A , CM000664.1:g.136873099G>A	GRCh37
NC_000002.10:g.136589569G>A	NCBI36
NG_011587.1:g.7627C>T , LRG_51:g.7627C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.387C>T	ENSP00000512428.1:p.Asp129=
ENST00000696137.1:c.354C>T	ENSP00000512429.1:p.Asp118=
ENST00000696152.1:c.354C>T	ENSP00000512443.1:p.Asp118=
ENST00000696228.1:c.387C>T	ENSP00000512494.1:p.Asp129=
ENST00000241393.4:c.399C>T MANE Select	ENSP00000241393.3:p.Asp133=
ENST00000241393.3:c.399C>T	ENSP00000241393.3:p.Asp133=
ENST00000409817.1:c.411C>T	ENSP00000386884.1:p.Asp137=
ENST00000466288.1:n.593C>T
NM_001008540.1:c.411C>T	NP_001008540.1:p.Asp137=
NM_003467.2:c.399C>T , LRG_51t1:c.399C>T	NP_003458.1:p.Asp133=
NM_001008540.2:c.411C>T	NP_001008540.1:p.Asp137=
NM_001348056.1:c.612C>T	NP_001334985.1:p.Asp204=
NM_001348059.1:c.498C>T	NP_001334988.1:p.Asp166=
NM_001348060.1:c.354C>T	NP_001334989.1:p.Asp118=
NM_001348056.2:c.612C>T	NP_001334985.1:p.Asp204=
NM_001348059.2:c.498C>T	NP_001334988.1:p.Asp166=
NM_001348060.2:c.354C>T	NP_001334989.1:p.Asp118=
NM_003467.3:c.399C>T MANE Select	NP_003458.1:p.Asp133=