Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71954918G>T , CM000674.2:g.71954918G>T | GRCh38 |
| NC_000012.11:g.72348698G>T , CM000674.1:g.72348698G>T | GRCh37 |
| NC_000012.10:g.70634965G>T | NCBI36 |
| NG_008279.1:g.21073G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173353.4:c.608+5263G>T MANE Select | NP_775489.2:n.608+5263G>T |
| ENST00000333850.4:c.608+5263G>T MANE Select | ENSP00000329093.3:n.608+5263G>T |
| NM_173353.3:c.608+5263G>T | NP_775489.2:n.608+5263G>T |
| ENST00000333850.3:c.608+5263G>T | ENSP00000329093.3:n.608+5263G>T |
| ENST00000546576.1:n.618+5263G>T | |
| XM_011537899.1:c.14+5263G>T | XP_011536201.1:n.14+5263G>T |
| XR_001748575.1:n.708+5263G>T | |
| XR_245894.2:n.708+5263G>T |