Canonical Allele Identifier: CA350522100
Gene: CXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs142978743
gnomAD v2: 2-219029088-T-C
gnomAD v4: 2-218164365-T-C
MyVariant Identifiers: chr2:g.219029088T>C (hg19) chr2:g.218164365T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164365T>C , CM000664.2:g.218164365T>C GRCh38
NC_000002.11:g.219029088T>C , CM000664.1:g.219029088T>C GRCh37
NC_000002.10:g.218737333T>C NCBI36
NG_011814.1:g.7629A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295683.3:c.847A>G MANE Select ENSP00000295683.2:p.Ile283Val
ENST00000295683.2:c.847A>G ENSP00000295683.2:p.Ile283Val
NM_000634.2:c.847A>G NP_000625.1:p.Ile283Val
NM_000634.3:c.847A>G MANE Select NP_000625.1:p.Ile283Val
Search 100 bp 5'
Search 100 bp 3'