Canonical Allele Identifier: CA348658723

Gene: CXCR4

Linked Data

• dbSNP Id: rs2104917315
• MyVariant Identifiers: chr2:g.136872995G>T (hg19) ; chr2:g.136115425G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115425G>T , CM000664.2:g.136115425G>T	GRCh38
NC_000002.11:g.136872995G>T , CM000664.1:g.136872995G>T	GRCh37
NC_000002.10:g.136589465G>T	NCBI36
NG_011587.1:g.7731C>A , LRG_51:g.7731C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.491C>A	ENSP00000512428.1:p.Thr164Asn
ENST00000696137.1:c.458C>A	ENSP00000512429.1:p.Thr153Asn
ENST00000696152.1:c.458C>A	ENSP00000512443.1:p.Thr153Asn
ENST00000696228.1:c.491C>A	ENSP00000512494.1:p.Thr164Asn
ENST00000241393.4:c.503C>A MANE Select	ENSP00000241393.3:p.Thr168Asn
ENST00000241393.3:c.503C>A	ENSP00000241393.3:p.Thr168Asn
ENST00000409817.1:c.515C>A	ENSP00000386884.1:p.Thr172Asn
ENST00000466288.1:n.697C>A
NM_001008540.1:c.515C>A	NP_001008540.1:p.Thr172Asn
NM_003467.2:c.503C>A , LRG_51t1:c.503C>A	NP_003458.1:p.Thr168Asn
NM_001008540.2:c.515C>A	NP_001008540.1:p.Thr172Asn
NM_001348056.1:c.716C>A	NP_001334985.1:p.Thr239Asn
NM_001348059.1:c.602C>A	NP_001334988.1:p.Thr201Asn
NM_001348060.1:c.458C>A	NP_001334989.1:p.Thr153Asn
NM_001348056.2:c.716C>A	NP_001334985.1:p.Thr239Asn
NM_001348059.2:c.602C>A	NP_001334988.1:p.Thr201Asn
NM_001348060.2:c.458C>A	NP_001334989.1:p.Thr153Asn
NM_003467.3:c.503C>A MANE Select	NP_003458.1:p.Thr168Asn