Canonical Allele Identifier: CA287188429
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs75565221
gnomAD v2: 17-4637735-C-T
gnomAD v3: 17-4734440-C-T
gnomAD v4: 17-4734440-C-T
MyVariant Identifiers: chr17:g.4637735C>T (hg19) chr17:g.4734440C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734440C>T , CM000679.2:g.4734440C>T GRCh38
NC_000017.10:g.4637735C>T , CM000679.1:g.4637735C>T GRCh37
NC_000017.9:g.4584484C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*63G>A MANE Select ENSP00000293778.7:n.*63G>A
ENST00000574412.6:c.*166G>A ENSP00000459592.2:n.*166G>A
ENST00000293778.10:c.*63G>A ENSP00000293778.6:n.*63G>A
ENST00000574412.5:c.*166G>A ENSP00000459592.1:n.*166G>A
ENST00000576153.5:n.619G>A
NM_022059.3:c.*63G>A NP_071342.2:n.*63G>A
NM_022059.4:c.*63G>A NP_071342.2:n.*63G>A
NM_001386809.1:c.*63G>A MANE Select NP_001373738.1:n.*63G>A
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