Canonical Allele Identifier: CA8309113
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs553816451
ExAC: 17:4637887 C / T
gnomAD v2: 17-4637887-C-T
gnomAD v3: 17-4734592-C-T
gnomAD v4: 17-4734592-C-T
MyVariant Identifiers: chr17:g.4637887C>T (hg19) chr17:g.4734592C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734592C>T , CM000679.2:g.4734592C>T GRCh38
NC_000017.10:g.4637887C>T , CM000679.1:g.4637887C>T GRCh37
NC_000017.9:g.4584636C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*14G>A MANE Select ENSP00000293778.7:n.*14G>A
ENST00000574412.6:c.*14G>A ENSP00000459592.2:n.*14G>A
ENST00000293778.10:c.*14G>A ENSP00000293778.6:n.*14G>A
ENST00000574412.5:c.*14G>A ENSP00000459592.1:n.*14G>A
ENST00000575168.1:n.610G>A
ENST00000576153.5:n.570G>A
NM_001100812.1:c.*14G>A NP_001094282.1:n.*14G>A
NM_022059.3:c.*14G>A NP_071342.2:n.*14G>A
NM_022059.4:c.*14G>A NP_071342.2:n.*14G>A
NM_001100812.2:c.*14G>A NP_001094282.2:n.*14G>A
NM_001386809.1:c.*14G>A MANE Select NP_001373738.1:n.*14G>A
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