Canonical Allele Identifier: CA350521902
Gene: CXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219028994T>G (hg19) chr2:g.218164271T>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000295683.3:c.941A>C MANE Select ENSP00000295683.2:p.His314Pro
ENST00000295683.2:c.941A>C ENSP00000295683.2:p.His314Pro
NM_000634.2:c.941A>C NP_000625.1:p.His314Pro
NM_000634.3:c.941A>C MANE Select NP_000625.1:p.His314Pro
Search 100 bp 5'
Search 100 bp 3'