Canonical Allele Identifier: CA2682013248

Linked Data

gnomAD v4: 7-22727066-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727066T>C , CM000669.2:g.22727066T>C GRCh38
NC_000007.13:g.22766685T>C , CM000669.1:g.22766685T>C GRCh37
NC_000007.12:g.22733210T>C NCBI36
NG_011640.1:g.4920T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+502A>G (STEAP1B)
ENST00000404625.5:c.-84-113T>C (IL6) ENSP00000385675.1:n.-84-113T>C
NR_131935.1:n.54-361A>G (IL6-AS1)
XM_011515390.1:c.-84-113T>C (IL6) XP_011513692.1:n.-84-113T>C
XM_011515390.2:c.-84-113T>C (IL6) XP_011513692.1:n.-84-113T>C