Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.101304141C>T , CM000665.2:g.101304141C>T | GRCh38 |
| NC_000003.11:g.101022985C>T , CM000665.1:g.101022985C>T | GRCh37 |
| NC_000003.10:g.102505675C>T | NCBI36 |
| NG_028284.1:g.21435G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016247.4:c.501+5G>A MANE Select | NP_057331.2:n.501+5G>A |
| ENST00000193391.8:c.501+5G>A MANE Select | ENSP00000193391.6:n.501+5G>A |
| NM_016247.3:c.501+5G>A | NP_057331.2:n.501+5G>A |
| ENST00000193391.7:c.501+5G>A | ENSP00000193391.6:n.501+5G>A |
| XM_011512871.1:c.207+5G>A | XP_011511173.1:n.207+5G>A |
| XM_011512872.1:c.90+5G>A | XP_011511174.1:n.90+5G>A |