Canonical Allele Identifier: CA2436523923

Gene: CXCR3

Genomic Alleles

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

Transcript Alleles

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