Canonical Allele Identifier: CA1328631481
Gene: CXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164274C= , CM000664.2:g.218164274C= GRCh38
NC_000002.11:g.219028997C= , CM000664.1:g.219028997C= GRCh37
NC_000002.10:g.218737242C= NCBI36
NG_011814.1:g.7720G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295683.3:c.938G= MANE Select ENSP00000295683.2:p.Arg313=
ENST00000295683.2:c.938G= ENSP00000295683.2:p.Arg313=
NM_000634.2:c.938G= NP_000625.1:p.Arg313=
NM_000634.3:c.938G= MANE Select NP_000625.1:p.Arg313=