Linked Data
ClinVar Variation Id:
2930107
ClinVar RCV Id:
RCV003787465
dbSNP Id:
rs1360721523
gnomAD v2:
2-20188963-A-G
gnomAD v4:
2-19989202-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.19989202A>G , CM000664.2:g.19989202A>G | GRCh38 |
| NC_000002.11:g.20188963A>G , CM000664.1:g.20188963A>G | GRCh37 |
| NC_000002.10:g.20052444A>G | NCBI36 |
| NG_021212.1:g.5922T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281405.9:c.105T>C MANE Select | ENSP00000281405.5:p.Asp35= | |
| ENST00000345530.8:c.105T>C MANE Plus Clinical | ENSP00000314444.5:p.Asp35= | |
| ENST00000281405.8:c.105T>C | ENSP00000281405.4:p.Asp35= | |
| ENST00000345530.7:c.105T>C | ENSP00000314444.5:p.Asp35= | |
| ENST00000414212.5:c.105T>C | ENSP00000390802.1:p.Asp35= | |
| NM_001006657.1:c.105T>C | NP_001006658.1:p.Asp35= | |
| NM_020779.3:c.105T>C | NP_065830.2:p.Asp35= | |
| XR_426989.2:n.138T>C | ||
| XR_939699.1:n.138T>C | ||
| XR_001738862.1:n.138T>C | ||
| XR_426989.3:n.138T>C | ||
| XR_939699.3:n.138T>C | ||
| NM_001006657.2:c.105T>C MANE Plus Clinical | NP_001006658.1:p.Asp35= | |
| NM_020779.4:c.105T>C MANE Select | NP_065830.2:p.Asp35= |