Canonical Allele Identifier: CA453973109

Linked Data

MyVariant Identifiers: chr7:g.22766054T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726435T>C , CM000669.2:g.22726435T>C GRCh38
NC_000007.13:g.22766054T>C , CM000669.1:g.22766054T>C GRCh37
NC_000007.12:g.22732579T>C NCBI36
NG_011640.1:g.4289T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+1133A>G (STEAP1B)
ENST00000404625.5:c.-85+177T>C (IL6) ENSP00000385675.1:n.-85+177T>C
NR_131935.1:n.324A>G (IL6-AS1)
XM_011515390.1:c.-85+177T>C (IL6) XP_011513692.1:n.-85+177T>C
XM_011515390.2:c.-85+177T>C (IL6) XP_011513692.1:n.-85+177T>C