HGVS | Genome Assembly |
---|---|
NC_000002.12:g.102349807T= , CM000664.2:g.102349807T= | GRCh38 |
NC_000002.11:g.102966267T= , CM000664.1:g.102966267T= | GRCh37 |
NC_000002.10:g.102332699T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000233954.6:c.1285+561T= (IL1RL1) MANE Select | ENSP00000233954.1:n.1285+561T= | |
ENST00000233954.5:c.1285+561T= (IL1RL1) | ENSP00000233954.1:n.1285+561T= | |
ENST00000410040.5:c.-28-12826T= (IL18R1) | ENSP00000386663.1:n.-28-12826T= | |
NM_016232.4:c.1285+561T= (IL1RL1) | NP_057316.3:n.1285+561T= | |
XM_006712839.2:c.1285+561T= (IL1RL1) | XP_006712902.1:n.1285+561T= | |
XM_006712839.3:c.1285+561T= (IL1RL1) | XP_006712902.1:n.1285+561T= | |
NM_016232.5:c.1285+561T= (IL1RL1) MANE Select | NP_057316.3:n.1285+561T= |