Canonical Allele Identifier: CA764849144

Gene: CXCR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218126282G>T , CM000664.2:g.218126282G>T	GRCh38
NC_000002.11:g.218991005G>T , CM000664.1:g.218991005G>T	GRCh37
NC_000002.10:g.218699250G>T	NCBI36
NG_052975.1:g.5993G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318507.7:c.-149G>T MANE Select	ENSP00000319635.2:n.-149G>T
ENST00000318507.6:c.-149G>T	ENSP00000319635.2:n.-149G>T
ENST00000415392.5:c.-140-9G>T	ENSP00000392348.1:n.-140-9G>T
ENST00000449014.5:c.-140-9G>T	ENSP00000410506.1:n.-140-9G>T
ENST00000453237.5:c.-140-9G>T	ENSP00000413686.1:n.-140-9G>T
ENST00000454148.1:c.-140-9G>T	ENSP00000415148.1:n.-140-9G>T
NM_001168298.1:c.-140-9G>T	NP_001161770.1:n.-140-9G>T
NM_001557.3:c.-149G>T	NP_001548.1:n.-149G>T
XM_005246530.2:c.-140-9G>T	XP_005246587.1:n.-140-9G>T
XM_005246530.3:c.-140-9G>T	XP_005246587.1:n.-140-9G>T
XM_017003990.1:c.-140-9G>T	XP_016859479.1:n.-140-9G>T
XM_017003992.1:c.-97G>T	XP_016859481.1:n.-97G>T
NM_001557.4:c.-149G>T MANE Select	NP_001548.1:n.-149G>T
NM_001168298.2:c.-140-9G>T	NP_001161770.1:n.-140-9G>T