Canonical Allele Identifier: CA431406257
Gene: CXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219028999A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164276A>G , CM000664.2:g.218164276A>G GRCh38
NC_000002.11:g.219028999A>G , CM000664.1:g.219028999A>G GRCh37
NC_000002.10:g.218737244A>G NCBI36
NG_011814.1:g.7718T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295683.3:c.936T>C MANE Select ENSP00000295683.2:p.Phe312=
ENST00000295683.2:c.936T>C ENSP00000295683.2:p.Phe312=
NM_000634.2:c.936T>C NP_000625.1:p.Phe312=
NM_000634.3:c.936T>C MANE Select NP_000625.1:p.Phe312=
Search 100 bp 5'
Search 100 bp 3'