Canonical Allele Identifier: CA1468311881

Gene: CXCL8

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73740952T>C , CM000666.2:g.73740952T>C	GRCh38
NC_000004.11:g.74606669T>C , CM000666.1:g.74606669T>C	GRCh37
NC_000004.10:g.74825533T>C	NCBI36
NG_029889.1:g.5447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696131.1:c.*171T>C	ENSP00000512424.1:n.*171T>C
ENST00000696132.1:c.*22+149T>C	ENSP00000512425.1:n.*22+149T>C
ENST00000307407.8:c.64+230T>C MANE Select	ENSP00000306512.3:n.64+230T>C
ENST00000307407.7:c.64+230T>C	ENSP00000306512.3:n.64+230T>C
ENST00000401931.1:c.64+230T>C	ENSP00000385908.1:n.64+230T>C
ENST00000483500.1:n.154+230T>C
NM_000584.3:c.64+230T>C	NP_000575.1:n.64+230T>C
NM_001354840.1:c.64+230T>C	NP_001341769.1:n.64+230T>C
NM_000584.4:c.64+230T>C MANE Select	NP_000575.1:n.64+230T>C
NM_001354840.2:c.64+230T>C	NP_001341769.1:n.64+230T>C
NM_001354840.3:c.64+230T>C	NP_001341769.1:n.64+230T>C