Linked Data
gnomAD v4:
1-40097329-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40097329T>C , CM000663.2:g.40097329T>C | GRCh38 |
| NC_000001.10:g.40563001T>C , CM000663.1:g.40563001T>C | GRCh37 |
| NC_000001.9:g.40335588T>C | NCBI36 |
| NG_009192.1:g.5142A>G , LRG_690:g.5142A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433473.7:c.-91A>G | ENSP00000394863.3:n.-91A>G | |
| NM_000310.3:c.-91A>G , LRG_690t1:c.-91A>G | NP_000301.1:n.-91A>G | |
| NM_001142604.1:c.-91A>G | NP_001136076.1:n.-91A>G | |
| NM_001363695.1:c.-91A>G | NP_001350624.1:n.-91A>G |