Canonical Allele Identifier: CA348657456

Gene: CXCR4

Linked Data

• dbSNP Id: rs147214773
• MyVariant Identifiers: chr2:g.136872495C>A (hg19) ; chr2:g.136114925C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136114925C>A , CM000664.2:g.136114925C>A	GRCh38
NC_000002.11:g.136872495C>A , CM000664.1:g.136872495C>A	GRCh37
NC_000002.10:g.136588965C>A	NCBI36
NG_011587.1:g.8231G>T , LRG_51:g.8231G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.991G>T	ENSP00000512428.1:p.Gly331Cys
ENST00000696137.1:c.958G>T	ENSP00000512429.1:p.Gly320Cys
ENST00000696152.1:c.958G>T	ENSP00000512443.1:p.Gly320Cys
ENST00000696228.1:c.991G>T	ENSP00000512494.1:p.Gly331Cys
ENST00000241393.4:c.1003G>T MANE Select	ENSP00000241393.3:p.Gly335Cys
ENST00000241393.3:c.1003G>T	ENSP00000241393.3:p.Gly335Cys
ENST00000409817.1:c.1015G>T	ENSP00000386884.1:p.Gly339Cys
ENST00000466288.1:n.1197G>T
NM_001008540.1:c.1015G>T	NP_001008540.1:p.Gly339Cys
NM_003467.2:c.1003G>T , LRG_51t1:c.1003G>T	NP_003458.1:p.Gly335Cys
NM_001008540.2:c.1015G>T	NP_001008540.1:p.Gly339Cys
NM_001348056.1:c.1216G>T	NP_001334985.1:p.Gly406Cys
NM_001348059.1:c.1102G>T	NP_001334988.1:p.Gly368Cys
NM_001348060.1:c.958G>T	NP_001334989.1:p.Gly320Cys
NM_001348056.2:c.1216G>T	NP_001334985.1:p.Gly406Cys
NM_001348059.2:c.1102G>T	NP_001334988.1:p.Gly368Cys
NM_001348060.2:c.958G>T	NP_001334989.1:p.Gly320Cys
NM_003467.3:c.1003G>T MANE Select	NP_003458.1:p.Gly335Cys