Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15180528T= , CM000681.2:g.15180528T= | GRCh38 |
| NC_000019.9:g.15291339T= , CM000681.1:g.15291339T= | GRCh37 |
| NC_000019.8:g.15152339T= | NCBI36 |
| NG_009819.1:g.25454A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.3142+153A= MANE Select | ENSP00000263388.1:n.3142+153A= | |
| ENST00000263388.6:c.3142+153A= | ENSP00000263388.1:n.3142+153A= | |
| ENST00000601011.1:c.2983+153A= | ENSP00000473138.1:n.2983+153A= | |
| NM_000435.2:c.3142+153A= | NP_000426.2:n.3142+153A= | |
| XM_005259924.3:c.2986+153A= | XP_005259981.1:n.2986+153A= | |
| XM_005259924.4:c.2986+153A= | XP_005259981.1:n.2986+153A= | |
| NM_000435.3:c.3142+153A= MANE Select | NP_000426.2:n.3142+153A= |