Canonical Allele Identifier: CA716220360

Gene: IL16

Linked Data

• dbSNP Id: rs1213744262
• gnomAD v3: 15-81296759-T-C
• gnomAD v4: 15-81296759-T-C
• MyVariant Identifiers: chr15:g.81589100T>C (hg19) ; chr15:g.81296759T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81296759T>C , CM000677.2:g.81296759T>C	GRCh38
NC_000015.9:g.81589100T>C , CM000677.1:g.81589100T>C	GRCh37
NC_000015.8:g.79376155T>C	NCBI36
NG_029933.1:g.104882T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302987.10:c.2044-169T>C	ENSP00000302935.5:n.2044-169T>C
ENST00000706926.1:c.1903-169T>C	ENSP00000516648.1:n.1903-169T>C
ENST00000302987.9:c.2044-169T>C	ENSP00000302935.5:n.2044-169T>C
ENST00000683961.1:c.1903-169T>C MANE Select	ENSP00000508085.1:n.1903-169T>C
ENST00000302987.8:c.1903-169T>C	ENSP00000302935.4:n.1903-169T>C
ENST00000360547.9:c.*1080-169T>C	ENSP00000456972.1:n.*1080-169T>C
ENST00000394660.6:c.1903-169T>C	ENSP00000378155.2:n.1903-169T>C
ENST00000560115.5:c.1873-169T>C
NM_001172128.1:c.1903-169T>C	NP_001165599.1:n.1903-169T>C
NM_172217.3:c.1903-169T>C	NP_757366.2:n.1903-169T>C
XM_005254342.2:c.2044-169T>C	XP_005254399.1:n.2044-169T>C
XM_005254346.3:c.-446T>C	XP_005254403.1:n.-446T>C
XM_011521518.1:c.1765-169T>C	XP_011519820.1:n.1765-169T>C
XM_011521519.1:c.1903-169T>C	XP_011519821.1:n.1903-169T>C
XM_011521520.1:c.1903-169T>C	XP_011519822.1:n.1903-169T>C
XR_931805.1:n.2004-169T>C
NM_001352684.1:c.73-169T>C	NP_001339613.1:n.73-169T>C
NM_001352685.1:c.1393-169T>C	NP_001339614.1:n.1393-169T>C
NM_001352686.1:c.2056-169T>C	NP_001339615.1:n.2056-169T>C
NM_172217.4:c.1903-169T>C	NP_757366.2:n.1903-169T>C
NR_148035.1:n.2279-169T>C
NM_001172128.2:c.1903-169T>C	NP_001165599.1:n.1903-169T>C
NM_001352684.2:c.73-169T>C	NP_001339613.1:n.73-169T>C
NM_001352685.2:c.1393-169T>C	NP_001339614.1:n.1393-169T>C
NM_172217.5:c.1903-169T>C MANE Select	NP_757366.2:n.1903-169T>C
NR_148035.2:n.2278-169T>C
NM_001352686.2:c.2056-169T>C	NP_001339615.1:n.2056-169T>C