Canonical Allele Identifier: CA350521906
Gene: CXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs61752206
gnomAD v4: 2-218164274-C-A
MyVariant Identifiers: chr2:g.219028997C>A (hg19) chr2:g.218164274C>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000295683.3:c.938G>T MANE Select ENSP00000295683.2:p.Arg313Leu
ENST00000295683.2:c.938G>T ENSP00000295683.2:p.Arg313Leu
NM_000634.2:c.938G>T NP_000625.1:p.Arg313Leu
NM_000634.3:c.938G>T MANE Select NP_000625.1:p.Arg313Leu
Search 100 bp 5'
Search 100 bp 3'