Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128261608C>T , CM000667.2:g.128261608C>T | GRCh38 |
| NC_000005.9:g.127597300C>T , CM000667.1:g.127597300C>T | GRCh37 |
| NC_000005.8:g.127625199C>T | NCBI36 |
| NG_008750.1:g.281436G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.8364+128G>A MANE Select | ENSP00000262464.4:n.8364+128G>A | |
| ENST00000262464.8:c.8364+128G>A | ENSP00000262464.4:n.8364+128G>A | |
| ENST00000508053.5:c.8364+128G>A | ENSP00000424571.1:n.8364+128G>A | |
| ENST00000619499.4:c.8361+128G>A | ENSP00000482132.1:n.8361+128G>A | |
| NM_001999.3:c.8364+128G>A | NP_001990.2:n.8364+128G>A | |
| XM_017009228.2:c.8211+128G>A | XP_016864717.1:n.8211+128G>A | |
| NM_001999.4:c.8364+128G>A MANE Select | NP_001990.2:n.8364+128G>A |