Canonical Allele Identifier: CA2190785531
Gene: IL16 HGNC NCBI

Linked Data

dbSNP Id: rs1895398077

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.81185033C>G , CM000677.2:g.81185033C>G GRCh38
NC_000015.9:g.81477374C>G , CM000677.1:g.81477374C>G GRCh37
NC_000015.8:g.79264429C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302987.10:c.40+2137C>G ENSP00000302935.5:n.40+2137C>G
ENST00000302987.9:c.40+2137C>G ENSP00000302935.5:n.40+2137C>G
ENST00000360547.9:c.-153+2137C>G ENSP00000456972.1:n.-153+2137C>G
ENST00000560241.5:c.-102+2137C>G ENSP00000452738.1:n.-102+2137C>G
XM_005254342.2:c.40+2137C>G XP_005254399.1:n.40+2137C>G