Linked Data
dbSNP Id:
rs114721034
gnomAD v2:
2-241812546-C-A
gnomAD v3:
2-240873129-C-A
gnomAD v4:
2-240873129-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240873129C>A , CM000664.2:g.240873129C>A | GRCh38 |
| NC_000002.11:g.241812546C>A , CM000664.1:g.241812546C>A | GRCh37 |
| NC_000002.10:g.241461219C>A | NCBI36 |
| NG_008005.1:g.9385C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.595+80C>A MANE Select | ENSP00000302620.3:n.595+80C>A | |
| ENST00000307503.3:c.595+80C>A | ENSP00000302620.3:n.595+80C>A | |
| ENST00000472436.1:n.695C>A | ||
| ENST00000476698.1:n.332+80C>A | ||
| NM_000030.2:c.595+80C>A | NP_000021.1:n.595+80C>A | |
| NM_000030.3:c.595+80C>A MANE Select | NP_000021.1:n.595+80C>A |