Linked Data
dbSNP Id:
rs1269170427
gnomAD v2:
4-100504666-C-G
gnomAD v3:
4-99583509-C-G
gnomAD v4:
4-99583509-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99583509C>G , CM000666.2:g.99583509C>G | GRCh38 |
| NC_000004.11:g.100504666C>G , CM000666.1:g.100504666C>G | GRCh37 |
| NC_000004.10:g.100723689C>G | NCBI36 |
| NG_011469.1:g.24427C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265517.10:c.385C>G MANE Select | ENSP00000265517.5:p.His129Asp | |
| ENST00000457717.6:c.385C>G | ENSP00000400821.1:p.His129Asp | |
| ENST00000511045.6:c.136C>G | ENSP00000427679.2:p.His46Asp | |
| ENST00000265517.9:c.385C>G | ENSP00000265517.5:p.His129Asp | |
| ENST00000422897.6:c.385C>G | ENSP00000407350.2:p.His129Asp | |
| ENST00000457717.5:c.385C>G | ENSP00000400821.1:p.His129Asp | |
| ENST00000506883.5:c.415C>G | ENSP00000426755.1:p.His139Asp | |
| ENST00000511045.5:c.466C>G | ENSP00000427679.1:p.His156Asp | |
| ENST00000619629.1:c.385C>G | ENSP00000482850.1:p.His129Asp | |
| NM_000253.3:c.385C>G | NP_000244.2:p.His129Asp | |
| NM_001300785.1:c.466C>G | NP_001287714.1:p.His156Asp | |
| NM_000253.4:c.385C>G | NP_000244.2:p.His129Asp | |
| NM_001300785.2:c.136C>G | NP_001287714.2:p.His46Asp | |
| NM_001386140.1:c.385C>G MANE Select | NP_001373069.1:p.His129Asp |