Canonical Allele Identifier: CA2682013341

Linked Data

gnomAD v4: 7-22727138-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727138A>C , CM000669.2:g.22727138A>C GRCh38
NC_000007.13:g.22766757A>C , CM000669.1:g.22766757A>C GRCh37
NC_000007.12:g.22733282A>C NCBI36
NG_011640.1:g.4992A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+430T>G (STEAP1B)
ENST00000404625.5:c.-84-41A>C (IL6) ENSP00000385675.1:n.-84-41A>C
NR_131935.1:n.53+430T>G (IL6-AS1)
XM_005249745.3:c.-125A>C (IL6) XP_005249802.1:n.-125A>C
XM_011515390.1:c.-84-41A>C (IL6) XP_011513692.1:n.-84-41A>C
XM_011515390.2:c.-84-41A>C (IL6) XP_011513692.1:n.-84-41A>C