Canonical Allele Identifier: CA348658732

Gene: CXCR4

Linked Data

• dbSNP Id: rs2104917323
• MyVariant Identifiers: chr2:g.136872996T>A (hg19) ; chr2:g.136115426T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115426T>A , CM000664.2:g.136115426T>A	GRCh38
NC_000002.11:g.136872996T>A , CM000664.1:g.136872996T>A	GRCh37
NC_000002.10:g.136589466T>A	NCBI36
NG_011587.1:g.7730A>T , LRG_51:g.7730A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.490A>T	ENSP00000512428.1:p.Thr164Ser
ENST00000696137.1:c.457A>T	ENSP00000512429.1:p.Thr153Ser
ENST00000696152.1:c.457A>T	ENSP00000512443.1:p.Thr153Ser
ENST00000696228.1:c.490A>T	ENSP00000512494.1:p.Thr164Ser
ENST00000241393.4:c.502A>T MANE Select	ENSP00000241393.3:p.Thr168Ser
ENST00000241393.3:c.502A>T	ENSP00000241393.3:p.Thr168Ser
ENST00000409817.1:c.514A>T	ENSP00000386884.1:p.Thr172Ser
ENST00000466288.1:n.696A>T
NM_001008540.1:c.514A>T	NP_001008540.1:p.Thr172Ser
NM_003467.2:c.502A>T , LRG_51t1:c.502A>T	NP_003458.1:p.Thr168Ser
NM_001008540.2:c.514A>T	NP_001008540.1:p.Thr172Ser
NM_001348056.1:c.715A>T	NP_001334985.1:p.Thr239Ser
NM_001348059.1:c.601A>T	NP_001334988.1:p.Thr201Ser
NM_001348060.1:c.457A>T	NP_001334989.1:p.Thr153Ser
NM_001348056.2:c.715A>T	NP_001334985.1:p.Thr239Ser
NM_001348059.2:c.601A>T	NP_001334988.1:p.Thr201Ser
NM_001348060.2:c.457A>T	NP_001334989.1:p.Thr153Ser
NM_003467.3:c.502A>T MANE Select	NP_003458.1:p.Thr168Ser