Canonical Allele Identifier: CA1328631483
Gene: CXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164277A= , CM000664.2:g.218164277A= GRCh38
NC_000002.11:g.219029000A= , CM000664.1:g.219029000A= GRCh37
NC_000002.10:g.218737245A= NCBI36
NG_011814.1:g.7717T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295683.3:c.935T= MANE Select ENSP00000295683.2:p.Phe312=
ENST00000295683.2:c.935T= ENSP00000295683.2:p.Phe312=
NM_000634.2:c.935T= NP_000625.1:p.Phe312=
NM_000634.3:c.935T= MANE Select NP_000625.1:p.Phe312=