Linked Data
ClinVar Variation Id:
532197
dbSNP Id:
rs147410912
ExAC:
20:18516299 G / T
gnomAD v2:
20-18516299-G-T
gnomAD v3:
20-18535655-G-T
gnomAD v4:
20-18535655-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.18535655G>T , CM000682.2:g.18535655G>T | GRCh38 |
| NC_000020.10:g.18516299G>T , CM000682.1:g.18516299G>T | GRCh37 |
| NC_000020.9:g.18464299G>T | NCBI36 |
| NG_016281.1:g.33112G>T | |
| NG_016281.2:g.33174G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336714.8:c.1317G>T | ENSP00000338844.3:p.Glu439Asp | |
| ENST00000377465.6:c.1317G>T | ENSP00000366685.1:p.Glu439Asp | |
| ENST00000643747.1:c.1263G>T | ENSP00000496460.1:p.Glu421Asp | |
| ENST00000650089.1:c.1317G>T MANE Select | ENSP00000497473.1:p.Glu439Asp | |
| ENST00000262544.6:c.1317G>T | ENSP00000262544.2:p.Glu439Asp | |
| ENST00000336714.7:c.1317G>T | ENSP00000338844.3:p.Glu439Asp | |
| ENST00000377465.5:c.1317G>T | ENSP00000366685.1:p.Glu439Asp | |
| ENST00000377475.7:c.1317G>T | ENSP00000366695.3:p.Glu439Asp | |
| NM_001172745.1:c.1317G>T | NP_001166216.1:p.Glu439Asp | |
| NM_001172746.1:c.1263G>T | NP_001166217.1:p.Glu421Asp | |
| NM_006363.4:c.1317G>T | NP_006354.2:p.Glu439Asp | |
| NM_032985.4:c.1317G>T | NP_116780.1:p.Glu439Asp | |
| NM_032986.3:c.1317G>T | NP_116781.1:p.Glu439Asp | |
| NM_001172745.2:c.1317G>T | NP_001166216.1:p.Glu439Asp | |
| NM_001172746.2:c.1263G>T | NP_001166217.1:p.Glu421Asp | |
| NM_006363.6:c.1317G>T MANE Select | NP_006354.2:p.Glu439Asp | |
| NM_032985.5:c.1317G>T | NP_116780.1:p.Glu439Asp | |
| NM_032986.4:c.1317G>T | NP_116781.1:p.Glu439Asp | |
| XM_017027593.1:c.1317G>T | XP_016883082.1:p.Glu439Asp | |
| NM_001172745.3:c.1317G>T | NP_001166216.1:p.Glu439Asp | |
| NM_001172746.3:c.1263G>T | NP_001166217.1:p.Glu421Asp | |
| NM_032985.6:c.1317G>T | NP_116780.1:p.Glu439Asp | |
| NM_032986.5:c.1317G>T | NP_116781.1:p.Glu439Asp |