Canonical Allele Identifier: CA350521913
Gene: CXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219029000A>C (hg19) chr2:g.218164277A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000295683.3:c.935T>G MANE Select ENSP00000295683.2:p.Phe312Cys
ENST00000295683.2:c.935T>G ENSP00000295683.2:p.Phe312Cys
NM_000634.2:c.935T>G NP_000625.1:p.Phe312Cys
NM_000634.3:c.935T>G MANE Select NP_000625.1:p.Phe312Cys
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