Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA11726849

Gene: CXCL9 HGNC NCBI
SDAD1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs10336

gnomAD v2: 4-76922988-A-G

gnomAD v3: 4-76001835-A-G

gnomAD v4: 4-76001835-A-G

MyVariant Identifiers: chr4:g.76922988A>G (hg19) chr4:g.76001835A>G (hg38)

JSON-LD

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76001835A>G , CM000666.2:g.76001835A>G	GRCh38
NC_000004.11:g.76922988A>G , CM000666.1:g.76922988A>G	GRCh37
NC_000004.10:g.77142012A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264888.6:c.*1763T>C (CXCL9) MANE Select	ENSP00000354901.4:n.*1763T>C
ENST00000264888.5:c.*1763T>C (CXCL9)	ENSP00000354901.4:n.*1763T>C
NM_002416.2:c.*1763T>C (CXCL9)	NP_002407.1:n.*1763T>C
NR_125906.1:n.816-3238A>G (SDAD1-AS1)
NM_002416.3:c.*1763T>C (CXCL9) MANE Select	NP_002407.1:n.*1763T>C

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