Linked Data
dbSNP Id:
rs772042724
ExAC:
12:110029051 A / G
gnomAD v2:
12-110029051-A-G
gnomAD v4:
12-109591246-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109591246A>G , CM000674.2:g.109591246A>G | GRCh38 |
| NC_000012.11:g.110029051A>G , CM000674.1:g.110029051A>G | GRCh37 |
| NC_000012.10:g.108513434A>G | NCBI36 |
| NG_007702.1:g.22552A>G , LRG_156:g.22552A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539696.6:c.-70A>G | ENSP00000439134.1:n.-70A>G | |
| ENST00000546277.6:c.774A>G | ENSP00000438153.2:p.Pro258= | |
| ENST00000636529.2:n.413A>G | ||
| ENST00000697195.1:c.*538A>G | ENSP00000513181.1:n.*538A>G | |
| ENST00000697196.1:c.862A>G | ENSP00000513182.1:p.Arg288Gly | |
| ENST00000697197.1:n.2803A>G | ||
| ENST00000228510.8:c.774A>G MANE Select | ENSP00000228510.3:p.Pro258= | |
| ENST00000636529.1:c.399A>G | ||
| ENST00000636996.1:c.622A>G | ||
| ENST00000228510.7:c.774A>G | ENSP00000228510.3:p.Pro258= | |
| ENST00000392727.7:c.618A>G | ENSP00000376487.3:p.Pro206= | |
| ENST00000447878.6:c.*221A>G | ENSP00000415555.2:n.*221A>G | |
| ENST00000537237.5:c.*447A>G | ENSP00000445382.1:n.*447A>G | |
| ENST00000539575.4:c.774A>G | ENSP00000443551.2:p.Pro258= | |
| ENST00000539696.5:c.-70A>G | ENSP00000439134.1:n.-70A>G | |
| ENST00000540353.1:n.3007A>G | ||
| ENST00000625889.2:c.618A>G | ENSP00000486846.1:p.Pro206= | |
| ENST00000629016.2:c.*221A>G | ENSP00000486804.1:n.*221A>G | |
| NM_000431.3:c.774A>G | NP_000422.1:p.Pro258= | |
| NM_001114185.2:c.774A>G | NP_001107657.1:p.Pro258= | |
| NM_001301182.1:c.618A>G | NP_001288111.1:p.Pro206= | |
| XM_011538372.1:c.774A>G | XP_011536674.1:p.Pro258= | |
| XM_017019313.2:c.618A>G | XP_016874802.1:p.Pro206= | |
| XM_017019314.1:c.774A>G | XP_016874803.1:p.Pro258= | |
| XM_024448982.1:c.774A>G | XP_024304750.1:p.Pro258= | |
| NM_000431.4:c.774A>G MANE Select | NP_000422.1:p.Pro258= | |
| NM_001114185.3:c.774A>G | NP_001107657.1:p.Pro258= | |
| NM_001301182.2:c.618A>G | NP_001288111.1:p.Pro206= |