Linked Data
gnomAD v4:
10-114044036-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044036C>A , CM000672.2:g.114044036C>A | GRCh38 |
| NC_000010.10:g.115803795C>A , CM000672.1:g.115803795C>A | GRCh37 |
| NC_000010.9:g.115793785C>A | NCBI36 |
| NG_012187.1:g.4990C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.-97C>A MANE Select | ENSP00000358301.2:n.-97C>A | |
| NM_000684.3:c.-97C>A MANE Select | NP_000675.1:n.-97C>A |