Linked Data
dbSNP Id:
rs80141609
gnomAD v2:
5-135230630-G-A
gnomAD v3:
5-135894941-G-A
gnomAD v4:
5-135894941-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135894941G>A , CM000667.2:g.135894941G>A | GRCh38 |
| NC_000005.9:g.135230630G>A , CM000667.1:g.135230630G>A | GRCh37 |
| NC_000005.8:g.135258529G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274520.2:c.183+499C>T MANE Select | ENSP00000274520.1:n.183+499C>T | |
| ENST00000274520.1:c.183+499C>T | ENSP00000274520.1:n.183+499C>T | |
| NM_000590.1:c.183+499C>T | NP_000581.1:n.183+499C>T | |
| NM_000590.2:c.183+499C>T MANE Select | NP_000581.1:n.183+499C>T |