Canonical Allele Identifier: CA917962270

Linked Data

dbSNP Id: rs1554299770

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726814_22726815delinsAA , CM000669.2:g.22726814_22726815delinsAA GRCh38
NC_000007.13:g.22766433_22766434delinsAA , CM000669.1:g.22766433_22766434delinsAA GRCh37
NC_000007.12:g.22732958_22732959delinsAA NCBI36
NG_011640.1:g.4668_4669delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+753_46+754delinsTT (STEAP1B)
ENST00000404625.5:c.-84-365_-84-364delinsAA (IL6) ENSP00000385675.1:n.-84-365_-84-364delinsAA
NR_131935.1:n.54-110_54-109delinsTT (IL6-AS1)
XM_011515390.1:c.-84-365_-84-364delinsAA (IL6) XP_011513692.1:n.-84-365_-84-364delinsAA
XM_011515390.2:c.-84-365_-84-364delinsAA (IL6) XP_011513692.1:n.-84-365_-84-364delinsAA