Canonical Allele Identifier: CA429206391

Gene: CXCR4

Linked Data

• dbSNP Id: rs1221712615
• MyVariant Identifiers: chr2:g.136872988G>C (hg19) ; chr2:g.136115418G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115418G>C , CM000664.2:g.136115418G>C	GRCh38
NC_000002.11:g.136872988G>C , CM000664.1:g.136872988G>C	GRCh37
NC_000002.10:g.136589458G>C	NCBI36
NG_011587.1:g.7738C>G , LRG_51:g.7738C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.498C>G	ENSP00000512428.1:p.Pro166=
ENST00000696137.1:c.465C>G	ENSP00000512429.1:p.Pro155=
ENST00000696152.1:c.465C>G	ENSP00000512443.1:p.Pro155=
ENST00000696228.1:c.498C>G	ENSP00000512494.1:p.Pro166=
ENST00000241393.4:c.510C>G MANE Select	ENSP00000241393.3:p.Pro170=
ENST00000241393.3:c.510C>G	ENSP00000241393.3:p.Pro170=
ENST00000409817.1:c.522C>G	ENSP00000386884.1:p.Pro174=
ENST00000466288.1:n.704C>G
NM_001008540.1:c.522C>G	NP_001008540.1:p.Pro174=
NM_003467.2:c.510C>G , LRG_51t1:c.510C>G	NP_003458.1:p.Pro170=
NM_001008540.2:c.522C>G	NP_001008540.1:p.Pro174=
NM_001348056.1:c.723C>G	NP_001334985.1:p.Pro241=
NM_001348059.1:c.609C>G	NP_001334988.1:p.Pro203=
NM_001348060.1:c.465C>G	NP_001334989.1:p.Pro155=
NM_001348056.2:c.723C>G	NP_001334985.1:p.Pro241=
NM_001348059.2:c.609C>G	NP_001334988.1:p.Pro203=
NM_001348060.2:c.465C>G	NP_001334989.1:p.Pro155=
NM_003467.3:c.510C>G MANE Select	NP_003458.1:p.Pro170=