Canonical Allele Identifier: CA1328618450

Gene: CXCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218136011T= , CM000664.2:g.218136011T=	GRCh38
NC_000002.11:g.219000734T= , CM000664.1:g.219000734T=	GRCh37
NC_000002.10:g.218708979T=	NCBI36
NG_052975.1:g.15722T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001557.4:c.*127T= MANE Select	NP_001548.1:n.*127T=
ENST00000318507.7:c.*127T= MANE Select	ENSP00000319635.2:n.*127T=
NM_001168298.1:c.*127T=	NP_001161770.1:n.*127T=
NM_001168298.2:c.*127T=	NP_001161770.1:n.*127T=
NM_001557.3:c.*127T=	NP_001548.1:n.*127T=
ENST00000318507.6:c.*127T=	ENSP00000319635.2:n.*127T=
XM_005246530.2:c.*127T=	XP_005246587.1:n.*127T=
XM_005246530.3:c.*127T=	XP_005246587.1:n.*127T=
XM_017003990.1:c.*127T=	XP_016859479.1:n.*127T=
XM_017003991.1:c.*127T=	XP_016859480.1:n.*127T=
XM_017003992.1:c.*127T=	XP_016859481.1:n.*127T=