Canonical Allele Identifier: CA2682013244

Linked Data

gnomAD v4: 7-22727063-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727063G>T , CM000669.2:g.22727063G>T GRCh38
NC_000007.13:g.22766682G>T , CM000669.1:g.22766682G>T GRCh37
NC_000007.12:g.22733207G>T NCBI36
NG_011640.1:g.4917G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+505C>A (STEAP1B)
ENST00000404625.5:c.-84-116G>T (IL6) ENSP00000385675.1:n.-84-116G>T
NR_131935.1:n.54-358C>A (IL6-AS1)
XM_011515390.1:c.-84-116G>T (IL6) XP_011513692.1:n.-84-116G>T
XM_011515390.2:c.-84-116G>T (IL6) XP_011513692.1:n.-84-116G>T