Canonical Allele Identifier: CA11208747
Gene: CXCR2 HGNC NCBI

Linked Data

dbSNP Id: rs6723449
gnomAD v2: 2-218997580-T-C
gnomAD v3: 2-218132857-T-C
gnomAD v4: 2-218132857-T-C
MyVariant Identifiers: chr2:g.218997580T>C (hg19) chr2:g.218132857T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218132857T>C , CM000664.2:g.218132857T>C GRCh38
NC_000002.11:g.218997580T>C , CM000664.1:g.218997580T>C GRCh37
NC_000002.10:g.218705825T>C NCBI36
NG_052975.1:g.12568T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318507.7:c.-25-1920T>C MANE Select ENSP00000319635.2:n.-25-1920T>C
ENST00000318507.6:c.-25-1920T>C ENSP00000319635.2:n.-25-1920T>C
ENST00000415392.5:c.-25-1920T>C ENSP00000392348.1:n.-25-1920T>C
ENST00000418878.1:c.-26+1855T>C ENSP00000416815.1:n.-26+1855T>C
ENST00000428565.1:c.-25-1920T>C ENSP00000392698.1:n.-25-1920T>C
ENST00000449014.5:c.-25-1920T>C ENSP00000410506.1:n.-25-1920T>C
ENST00000453237.5:c.-25-1920T>C ENSP00000413686.1:n.-25-1920T>C
ENST00000454148.1:c.-25-1920T>C ENSP00000415148.1:n.-25-1920T>C
NM_001168298.1:c.-25-1920T>C NP_001161770.1:n.-25-1920T>C
NM_001557.3:c.-25-1920T>C NP_001548.1:n.-25-1920T>C
XM_005246530.2:c.-25-1920T>C XP_005246587.1:n.-25-1920T>C
XM_005246530.3:c.-25-1920T>C XP_005246587.1:n.-25-1920T>C
XM_017003990.1:c.-25-1920T>C XP_016859479.1:n.-25-1920T>C
XM_017003991.1:c.-25-1920T>C XP_016859480.1:n.-25-1920T>C
XM_017003992.1:c.-25-1920T>C XP_016859481.1:n.-25-1920T>C
NM_001557.4:c.-25-1920T>C MANE Select NP_001548.1:n.-25-1920T>C
NM_001168298.2:c.-25-1920T>C NP_001161770.1:n.-25-1920T>C
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