Canonical Allele Identifier: CA15008482
Gene: CXCR3 HGNC NCBI
MyVariant.info:
GRCh38 chrX:g.71618204C>T
GRCh37 chrX:g.70838054C>T
gnomAD v2:
X:70838054 C / T
gnomAD v3:
X:71618204 C / T
gnomAD v4:
chrX-71618204-C-T
Joint Max Group AF 0.36644911 (SAS)
Genomes Max Group AF 0.35923895 (SAS)
Exomes Max Group AF 0.41329268 (SAS)
dbSNP:
2280964
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71618204C>T , CM000685.2:g.71618204C>T GRCh38
NC_000023.10:g.70838054C>T , CM000685.1:g.70838054C>T GRCh37
NC_000023.9:g.70754779C>T NCBI36
NG_029076.1:g.5314G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373693.4:c.12+234G>A MANE Select ENSP00000362797.3:n.12+234G>A
ENST00000373691.4:c.-92+234G>A ENSP00000362795.4:n.-92+234G>A
ENST00000373693.3:c.12+234G>A ENSP00000362797.3:n.12+234G>A
NM_001142797.1:c.-92+234G>A NP_001136269.1:n.-92+234G>A
NM_001504.1:c.12+234G>A NP_001495.1:n.12+234G>A
XM_005262256.2:c.42+127G>A XP_005262313.1:n.42+127G>A
XM_005262257.2:c.42+127G>A XP_005262314.1:n.42+127G>A
XM_005262256.3:c.42+127G>A XP_005262313.1:n.42+127G>A
XM_005262257.3:c.42+127G>A XP_005262314.1:n.42+127G>A
XM_017029435.1:c.-92+127G>A XP_016884924.1:n.-92+127G>A
XM_017029436.1:c.12+234G>A XP_016884925.1:n.12+234G>A
NM_001504.2:c.12+234G>A MANE Select NP_001495.1:n.12+234G>A
NM_001142797.2:c.-92+234G>A NP_001136269.1:n.-92+234G>A
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