Canonical Allele Identifier: CA350521889
Gene: CXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219028988A>C (hg19) chr2:g.218164265A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164265A>C , CM000664.2:g.218164265A>C GRCh38
NC_000002.11:g.219028988A>C , CM000664.1:g.219028988A>C GRCh37
NC_000002.10:g.218737233A>C NCBI36
NG_011814.1:g.7729T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295683.3:c.947T>G MANE Select ENSP00000295683.2:p.Phe316Cys
ENST00000295683.2:c.947T>G ENSP00000295683.2:p.Phe316Cys
NM_000634.2:c.947T>G NP_000625.1:p.Phe316Cys
NM_000634.3:c.947T>G MANE Select NP_000625.1:p.Phe316Cys
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