Linked Data
dbSNP Id:
rs966977603
gnomAD v4:
1-40097448-C-A
MyVariant Identifiers:
chr1:g.40097448C>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40097448C>A , CM000663.2:g.40097448C>A | GRCh38 |
| NC_000001.10:g.40563120C>A , CM000663.1:g.40563120C>A | GRCh37 |
| NC_000001.9:g.40335707C>A | NCBI36 |
| NG_009192.1:g.5023G>T , LRG_690:g.5023G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433473.7:c.-210G>T | ENSP00000394863.3:n.-210G>T | |
| NM_000310.3:c.-210G>T , LRG_690t1:c.-210G>T | NP_000301.1:n.-210G>T | |
| NM_001142604.1:c.-210G>T | NP_001136076.1:n.-210G>T | |
| NM_001363695.1:c.-210G>T | NP_001350624.1:n.-210G>T |