Canonical Allele Identifier: CA2101903
Gene: CXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs571690138
ExAC: 2:219028994 T / C
gnomAD v2: 2-219028994-T-C
gnomAD v4: 2-218164271-T-C
MyVariant Identifiers: chr2:g.219028994T>C (hg19) chr2:g.218164271T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164271T>C , CM000664.2:g.218164271T>C GRCh38
NC_000002.11:g.219028994T>C , CM000664.1:g.219028994T>C GRCh37
NC_000002.10:g.218737239T>C NCBI36
NG_011814.1:g.7723A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295683.3:c.941A>G MANE Select ENSP00000295683.2:p.His314Arg
ENST00000295683.2:c.941A>G ENSP00000295683.2:p.His314Arg
NM_000634.2:c.941A>G NP_000625.1:p.His314Arg
NM_000634.3:c.941A>G MANE Select NP_000625.1:p.His314Arg
Search 100 bp 5'
Search 100 bp 3'