Canonical Allele Identifier: CA14185102
Gene: IL16 HGNC NCBI

Linked Data

dbSNP Id: rs4778889
gnomAD v2: 15-81588995-T-C
gnomAD v3: 15-81296654-T-C
gnomAD v4: 15-81296654-T-C
MyVariant Identifiers: chr15:g.81588995T>C (hg19) chr15:g.81296654T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.81296654T>C , CM000677.2:g.81296654T>C GRCh38
NC_000015.9:g.81588995T>C , CM000677.1:g.81588995T>C GRCh37
NC_000015.8:g.79376050T>C NCBI36
NG_029933.1:g.104777T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302987.10:c.2044-274T>C ENSP00000302935.5:n.2044-274T>C
ENST00000706926.1:c.1903-274T>C ENSP00000516648.1:n.1903-274T>C
ENST00000302987.9:c.2044-274T>C ENSP00000302935.5:n.2044-274T>C
ENST00000683961.1:c.1903-274T>C MANE Select ENSP00000508085.1:n.1903-274T>C
ENST00000302987.8:c.1903-274T>C ENSP00000302935.4:n.1903-274T>C
ENST00000360547.9:c.*1080-274T>C ENSP00000456972.1:n.*1080-274T>C
ENST00000394660.6:c.1903-274T>C ENSP00000378155.2:n.1903-274T>C
ENST00000560115.5:c.1873-274T>C
NM_001172128.1:c.1903-274T>C NP_001165599.1:n.1903-274T>C
NM_172217.3:c.1903-274T>C NP_757366.2:n.1903-274T>C
XM_005254342.2:c.2044-274T>C XP_005254399.1:n.2044-274T>C
XM_005254346.3:c.-551T>C XP_005254403.1:n.-551T>C
XM_011521518.1:c.1765-274T>C XP_011519820.1:n.1765-274T>C
XM_011521519.1:c.1903-274T>C XP_011519821.1:n.1903-274T>C
XM_011521520.1:c.1903-274T>C XP_011519822.1:n.1903-274T>C
XR_931805.1:n.2004-274T>C
NM_001352684.1:c.73-274T>C NP_001339613.1:n.73-274T>C
NM_001352685.1:c.1393-274T>C NP_001339614.1:n.1393-274T>C
NM_001352686.1:c.2056-274T>C NP_001339615.1:n.2056-274T>C
NM_172217.4:c.1903-274T>C NP_757366.2:n.1903-274T>C
NR_148035.1:n.2279-274T>C
NM_001172128.2:c.1903-274T>C NP_001165599.1:n.1903-274T>C
NM_001352684.2:c.73-274T>C NP_001339613.1:n.73-274T>C
NM_001352685.2:c.1393-274T>C NP_001339614.1:n.1393-274T>C
NM_172217.5:c.1903-274T>C MANE Select NP_757366.2:n.1903-274T>C
NR_148035.2:n.2278-274T>C
NM_001352686.2:c.2056-274T>C NP_001339615.1:n.2056-274T>C
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