Linked Data
dbSNP Id:
rs2058975463
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868931C>G , CM000664.2:g.240868931C>G | GRCh38 |
| NC_000002.11:g.241808348C>G , CM000664.1:g.241808348C>G | GRCh37 |
| NC_000002.10:g.241457021C>G | NCBI36 |
| NG_008005.1:g.5187C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.66C>G MANE Select | ENSP00000302620.3:p.Asn22Lys | |
| ENST00000307503.3:c.66C>G | ENSP00000302620.3:p.Asn22Lys | |
| ENST00000472436.1:n.86C>G | ||
| NM_000030.2:c.66C>G | NP_000021.1:p.Asn22Lys | |
| XR_924060.1:n.405+1302G>C | ||
| NM_000030.3:c.66C>G MANE Select | NP_000021.1:p.Asn22Lys |