Canonical Allele Identifier: CA99815742
Gene: CXCL9 HGNC NCBI
SDAD1-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.76002845G>A
GRCh37 chr4:g.76923998G>A
gnomAD v2:
4:76923998 G / A
gnomAD v3:
4:76002845 G / A
gnomAD v4:
chr4-76002845-G-A
Joint Max Group AF 0.27592407 (AFR)
Genomes Max Group AF 0.27596963 (AFR)
Exomes Max Group AF 0.15929546 (AFR)
dbSNP:
3733236
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76002845G>A , CM000666.2:g.76002845G>A GRCh38
NC_000004.11:g.76923998G>A , CM000666.1:g.76923998G>A GRCh37
NC_000004.10:g.77143022G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264888.6:c.*753C>T (CXCL9) MANE Select ENSP00000354901.4:n.*753C>T
ENST00000264888.5:c.*753C>T (CXCL9) ENSP00000354901.4:n.*753C>T
NM_002416.2:c.*753C>T (CXCL9) NP_002407.1:n.*753C>T
NR_125906.1:n.816-2228G>A (SDAD1-AS1)
NM_002416.3:c.*753C>T (CXCL9) MANE Select NP_002407.1:n.*753C>T
Search 100 bp 5'
Search 100 bp 3'