Linked Data
dbSNP Id:
rs201115819
ExAC:
12:9221407 G / A
gnomAD v2:
12-9221407-G-A
gnomAD v3:
12-9068811-G-A
gnomAD v4:
12-9068811-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.9068811G>A , CM000674.2:g.9068811G>A | GRCh38 |
| NC_000012.11:g.9221407G>A , CM000674.1:g.9221407G>A | GRCh37 |
| NC_000012.10:g.9112674G>A | NCBI36 |
| NG_011717.1:g.52152C>T | |
| NG_011717.2:g.52152C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318602.12:c.4295C>T (A2M) MANE Select | ENSP00000323929.8:p.Thr1432Met | |
| ENST00000318602.11:c.4295C>T (A2M) | ENSP00000323929.7:p.Thr1432Met | |
| ENST00000495442.1:n.145C>T (A2M) | ||
| ENST00000495709.1:n.268C>T (A2M) | ||
| ENST00000543436.2:n.452-999C>T (A2M) | ||
| NM_000014.4:c.4295C>T (A2M) | NP_000005.2:p.Thr1432Met | |
| XM_006719056.2:c.4295C>T (A2M) | XP_006719119.1:p.Thr1432Met | |
| NM_000014.5:c.4295C>T (A2M) | NP_000005.2:p.Thr1432Met | |
| NM_001347423.1:c.4295C>T (A2M) | NP_001334352.1:p.Thr1432Met | |
| NM_001347424.1:c.3995C>T (A2M) | NP_001334353.1:p.Thr1332Met | |
| NM_001347425.1:c.3845C>T (A2M) | NP_001334354.1:p.Thr1282Met | |
| XM_006719056.3:c.4295C>T (A2M) | XP_006719119.1:p.Thr1432Met | |
| XM_017018683.1:c.*33+10645G>A (KLRG1) | XP_016874172.1:n.*33+10645G>A | |
| XM_017018684.1:c.*33+10645G>A (KLRG1) | XP_016874173.1:n.*33+10645G>A | |
| XM_017018685.1:c.*33+10645G>A (KLRG1) | XP_016874174.1:n.*33+10645G>A | |
| NM_000014.6:c.4295C>T (A2M) MANE Select | NP_000005.3:p.Thr1432Met | |
| NM_001347423.2:c.4295C>T (A2M) | NP_001334352.2:p.Thr1432Met | |
| NM_001347424.2:c.3995C>T (A2M) | NP_001334353.2:p.Thr1332Met | |
| NM_001347425.2:c.3845C>T (A2M) | NP_001334354.2:p.Thr1282Met |