Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.44372958C= , CM000667.2:g.44372958C= | GRCh38 |
| NC_000005.9:g.44373060C= , CM000667.1:g.44373060C= | GRCh37 |
| NC_000005.8:g.44408817C= | NCBI36 |
| NG_011446.1:g.20725G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004465.2:c.325+15400G= MANE Select | NP_004456.1:n.325+15400G= |
| ENST00000264664.5:c.325+15400G= MANE Select | ENSP00000264664.4:n.325+15400G= |
| NM_004465.1:c.325+15400G= | NP_004456.1:n.325+15400G= |
| ENST00000264664.4:c.325+15400G= | ENSP00000264664.4:n.325+15400G= |
| XM_005248264.2:c.325+15400G= | XP_005248321.1:n.325+15400G= |
| XM_005248264.4:c.325+15400G= | XP_005248321.1:n.325+15400G= |