Canonical Allele Identifier: CA350521903
Gene: CXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1691238362
MyVariant Identifiers: chr2:g.219028995G>A (hg19) chr2:g.218164272G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218164272G>A , CM000664.2:g.218164272G>A GRCh38
NC_000002.11:g.219028995G>A , CM000664.1:g.219028995G>A GRCh37
NC_000002.10:g.218737240G>A NCBI36
NG_011814.1:g.7722C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295683.3:c.940C>T MANE Select ENSP00000295683.2:p.His314Tyr
ENST00000295683.2:c.940C>T ENSP00000295683.2:p.His314Tyr
NM_000634.2:c.940C>T NP_000625.1:p.His314Tyr
NM_000634.3:c.940C>T MANE Select NP_000625.1:p.His314Tyr
Search 100 bp 5'
Search 100 bp 3'