Linked Data
ClinVar Variation Id:
198408
dbSNP Id:
rs145037134
ExAC:
10:90983507 T / G
gnomAD v2:
10-90983507-T-G
gnomAD v3:
10-89223750-T-G
gnomAD v4:
10-89223750-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89223750T>G , CM000672.2:g.89223750T>G | GRCh38 |
| NC_000010.10:g.90983507T>G , CM000672.1:g.90983507T>G | GRCh37 |
| NC_000010.9:g.90973487T>G | NCBI36 |
| NG_008194.1:g.33154A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000336233.10:c.756A>C MANE Select | ENSP00000337354.5:p.Ile252= | |
| ENST00000336233.9:c.756A>C | ENSP00000337354.5:p.Ile252= | |
| ENST00000371837.5:c.588A>C | ENSP00000360903.1:p.Ile196= | |
| ENST00000428800.5:c.756A>C | ENSP00000388415.1:p.Ile252= | |
| ENST00000456827.5:c.408A>C | ENSP00000413019.2:p.Ile136= | |
| NM_000235.3:c.756A>C | NP_000226.2:p.Ile252= | |
| NM_001127605.2:c.756A>C | NP_001121077.1:p.Ile252= | |
| NM_001288979.1:c.408A>C | NP_001275908.1:p.Ile136= | |
| XM_024448023.1:c.756A>C | XP_024303791.1:p.Ile252= | |
| NM_000235.4:c.756A>C MANE Select | NP_000226.2:p.Ile252= | |
| NM_001127605.3:c.756A>C | NP_001121077.1:p.Ile252= | |
| NM_001288979.2:c.408A>C | NP_001275908.1:p.Ile136= |