Canonical Allele Identifier: CA716134804

Gene: IL16

Linked Data

• dbSNP Id: rs1182907597
• gnomAD v3: 15-81185141-C-T
• gnomAD v4: 15-81185141-C-T
• MyVariant Identifiers: chr15:g.81477482C>T (hg19) ; chr15:g.81185141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.81185141C>T , CM000677.2:g.81185141C>T	GRCh38
NC_000015.9:g.81477482C>T , CM000677.1:g.81477482C>T	GRCh37
NC_000015.8:g.79264537C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000302987.10:c.40+2245C>T	ENSP00000302935.5:n.40+2245C>T
ENST00000302987.9:c.40+2245C>T	ENSP00000302935.5:n.40+2245C>T
ENST00000360547.9:c.-153+2245C>T	ENSP00000456972.1:n.-153+2245C>T
ENST00000560241.5:c.-102+2245C>T	ENSP00000452738.1:n.-102+2245C>T
XM_005254342.2:c.40+2245C>T	XP_005254399.1:n.40+2245C>T