Linked Data
dbSNP Id:
rs935421791
gnomAD v2:
18-60985998-T-C
gnomAD v3:
18-63318765-T-C
gnomAD v4:
18-63318765-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.63318765T>C , CM000680.2:g.63318765T>C | GRCh38 |
| NC_000018.9:g.60985998T>C , CM000680.1:g.60985998T>C | GRCh37 |
| NC_000018.8:g.59136978T>C | NCBI36 |
| NG_009361.1:g.5616A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333681.5:c.-99A>G MANE Select | ENSP00000329623.3:n.-99A>G | |
| ENST00000333681.4:c.-99A>G | ENSP00000329623.3:n.-99A>G | |
| ENST00000398117.1:c.-99A>G | ENSP00000381185.1:n.-99A>G | |
| ENST00000589955.2:c.-99A>G | ENSP00000466417.1:n.-99A>G | |
| NM_000633.2:c.-99A>G | NP_000624.2:n.-99A>G | |
| NM_000657.2:c.-99A>G | NP_000648.2:n.-99A>G | |
| XM_011526135.1:c.-99A>G | XP_011524437.1:n.-99A>G | |
| XR_935246.1:n.1014A>G | ||
| XR_935247.1:n.1014A>G | ||
| XR_935248.1:n.793A>G | ||
| XM_011526135.3:c.-99A>G | XP_011524437.1:n.-99A>G | |
| XM_017025917.2:c.-99A>G | XP_016881406.1:n.-99A>G | |
| XR_935248.3:n.1295A>G | ||
| NM_000633.3:c.-99A>G MANE Select | NP_000624.2:n.-99A>G | |
| NM_000657.3:c.-99A>G | NP_000648.2:n.-99A>G |