Canonical Allele Identifier: CA429206440

Gene: CXCR4

Linked Data

• dbSNP Id: rs1684863069
• gnomAD v4: 2-136115604-T-C
• MyVariant Identifiers: chr2:g.136873174T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115604T>C , CM000664.2:g.136115604T>C	GRCh38
NC_000002.11:g.136873174T>C , CM000664.1:g.136873174T>C	GRCh37
NC_000002.10:g.136589644T>C	NCBI36
NG_011587.1:g.7552A>G , LRG_51:g.7552A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.312A>G	ENSP00000512428.1:p.Leu104=
ENST00000696137.1:c.279A>G	ENSP00000512429.1:p.Leu93=
ENST00000696152.1:c.279A>G	ENSP00000512443.1:p.Leu93=
ENST00000696228.1:c.312A>G	ENSP00000512494.1:p.Leu104=
ENST00000241393.4:c.324A>G MANE Select	ENSP00000241393.3:p.Leu108=
ENST00000241393.3:c.324A>G	ENSP00000241393.3:p.Leu108=
ENST00000409817.1:c.336A>G	ENSP00000386884.1:p.Leu112=
ENST00000466288.1:n.518A>G
NM_001008540.1:c.336A>G	NP_001008540.1:p.Leu112=
NM_003467.2:c.324A>G , LRG_51t1:c.324A>G	NP_003458.1:p.Leu108=
NM_001008540.2:c.336A>G	NP_001008540.1:p.Leu112=
NM_001348056.1:c.537A>G	NP_001334985.1:p.Leu179=
NM_001348059.1:c.423A>G	NP_001334988.1:p.Leu141=
NM_001348060.1:c.279A>G	NP_001334989.1:p.Leu93=
NM_001348056.2:c.537A>G	NP_001334985.1:p.Leu179=
NM_001348059.2:c.423A>G	NP_001334988.1:p.Leu141=
NM_001348060.2:c.279A>G	NP_001334989.1:p.Leu93=
NM_003467.3:c.324A>G MANE Select	NP_003458.1:p.Leu108=