Linked Data
gnomAD v4:
2-202556352-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202556352A>G , CM000664.2:g.202556352A>G | GRCh38 |
| NC_000002.11:g.203421075A>G , CM000664.1:g.203421075A>G | GRCh37 |
| NC_000002.10:g.203129320A>G | NCBI36 |
| NG_009363.1:g.185026A>G , LRG_712:g.185026A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.2687A>G MANE Select | ENSP00000363708.4:p.Glu896Gly | |
| ENST00000638587.1:c.2618A>G | ENSP00000491062.1:n.2618A>G | |
| ENST00000374574.2:c.1587-3344A>G | ENSP00000363702.2:n.1587-3344A>G | |
| ENST00000374580.8:c.2687A>G | ENSP00000363708.4:p.Glu896Gly | |
| NM_001204.6:c.2687A>G , LRG_712t1:c.2687A>G | NP_001195.2:p.Glu896Gly | |
| XM_011511687.1:c.2687A>G | XP_011509989.1:p.Glu896Gly | |
| XM_011511688.1:c.1587-3344A>G | XP_011509990.1:n.1587-3344A>G | |
| NM_001204.7:c.2687A>G MANE Select | NP_001195.2:p.Glu896Gly |