Linked Data
ClinVar Variation Id:
2861690
ClinVar RCV Id:
RCV003704461
MyVariant Identifiers:
chrX:g.107911640T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108668410T>C , CM000685.2:g.108668410T>C | GRCh38 |
| NC_000023.10:g.107911640T>C , CM000685.1:g.107911640T>C | GRCh37 |
| NC_000023.9:g.107798296T>C | NCBI36 |
| NG_011977.1:g.233487T>C | |
| NG_011977.2:g.233487T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000328300.11:c.3696T>C MANE Select | ENSP00000331902.7:p.Gly1232= | |
| ENST00000361603.7:c.3696T>C | ENSP00000354505.2:p.Gly1232= | |
| ENST00000328300.10:c.3696T>C | ENSP00000331902.6:p.Gly1232= | |
| ENST00000361603.6:c.3696T>C | ENSP00000354505.2:p.Gly1232= | |
| NM_000495.4:c.3696T>C | NP_000486.1:p.Gly1232= | |
| NM_033380.2:c.3696T>C | NP_203699.1:p.Gly1232= | |
| XM_005262070.2:c.3696T>C | XP_005262127.1:p.Gly1232= | |
| XM_006724616.2:c.3696T>C | XP_006724679.1:p.Gly1232= | |
| XM_011530849.1:c.3372T>C | XP_011529151.1:p.Gly1124= | |
| XM_011530850.1:c.3696T>C | XP_011529152.1:p.Gly1232= | |
| XM_011530851.1:c.1269T>C | XP_011529153.1:p.Gly423= | |
| XM_011530849.2:c.3711T>C | XP_011529151.2:p.Gly1237= | |
| XM_017029259.2:c.3711T>C | XP_016884748.1:p.Gly1237= | |
| XM_017029260.1:c.3711T>C | XP_016884749.1:p.Gly1237= | |
| XM_017029261.1:c.3711T>C | XP_016884750.1:p.Gly1237= | |
| XM_017029262.2:c.3711T>C | XP_016884751.1:p.Gly1237= | |
| XM_017029263.2:c.2031T>C | XP_016884752.1:p.Gly677= | |
| NM_000495.5:c.3696T>C | NP_000486.1:p.Gly1232= | |
| NM_033380.3:c.3696T>C MANE Select | NP_203699.1:p.Gly1232= |