Canonical Allele Identifier: CA2101902
Gene: CXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs571690138
ExAC: 2:219028994 T / A
gnomAD v2: 2-219028994-T-A
gnomAD v3: 2-218164271-T-A
gnomAD v4: 2-218164271-T-A
MyVariant Identifiers: chr2:g.219028994T>A (hg19) chr2:g.218164271T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000295683.3:c.941A>T MANE Select ENSP00000295683.2:p.His314Leu
ENST00000295683.2:c.941A>T ENSP00000295683.2:p.His314Leu
NM_000634.2:c.941A>T NP_000625.1:p.His314Leu
NM_000634.3:c.941A>T MANE Select NP_000625.1:p.His314Leu
Search 100 bp 5'
Search 100 bp 3'