Canonical Allele Identifier: CA497526092
Gene: CXCL16 HGNC NCBI

Linked Data

COSMIC: COSM3378233 COSM3378234
MyVariant Identifiers: chr17:g.4637925A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734630A>C , CM000679.2:g.4734630A>C GRCh38
NC_000017.10:g.4637925A>C , CM000679.1:g.4637925A>C GRCh37
NC_000017.9:g.4584674A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.741T>G MANE Select ENSP00000293778.7:p.Pro247=
ENST00000574412.6:c.741T>G ENSP00000459592.2:p.Pro247=
ENST00000293778.10:c.798T>G ENSP00000293778.6:p.Pro266=
ENST00000574412.5:c.798T>G ENSP00000459592.1:p.Pro266=
ENST00000575168.1:n.572T>G
ENST00000576153.5:n.532T>G
NM_001100812.1:c.798T>G NP_001094282.1:p.Pro266=
NM_022059.3:c.798T>G NP_071342.2:p.Pro266=
NM_022059.4:c.798T>G NP_071342.2:p.Pro266=
NM_001100812.2:c.741T>G NP_001094282.2:p.Pro247=
NM_001386809.1:c.741T>G MANE Select NP_001373738.1:p.Pro247=
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