Linked Data
dbSNP Id:
rs1294151567
gnomAD v2:
X-41333841-G-A
gnomAD v4:
X-41474588-G-A
COSMIC:
COSM5500305
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.41474588G>A , CM000685.2:g.41474588G>A | GRCh38 |
| NC_000023.10:g.41333841G>A , CM000685.1:g.41333841G>A | GRCh37 |
| NC_000023.9:g.41218785G>A | NCBI36 |
| NG_009112.1:g.32129G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342595.3:c.1120G>A | ENSP00000340328.3:p.Gly374Arg | |
| ENST00000378220.3:c.1120G>A MANE Select | ENSP00000367465.2:p.Gly374Arg | |
| ENST00000378220.2:c.1135G>A | ENSP00000367465.1:p.Gly379Arg | |
| ENST00000342595.2:c.1135G>A | ENSP00000340328.2:p.Gly379Arg | |
| ENST00000378220.1:c.1135G>A | ENSP00000367465.1:p.Gly379Arg | |
| NM_022567.2:c.1135G>A | NP_072089.1:p.Gly379Arg | |
| XM_005272632.2:c.1135G>A | XP_005272689.1:p.Gly379Arg | |
| XM_017029709.1:c.1135G>A | XP_016885198.1:p.Gly379Arg | |
| NM_001378477.3:c.1120G>A MANE Select | NP_001365406.2:p.Gly374Arg | |
| NM_022567.3:c.1120G>A | NP_072089.2:p.Gly374Arg |