Canonical Allele Identifier: CA2554107670

Genomic Alleles

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

Transcript Alleles

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