Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045627T>C , CM000675.2:g.48045627T>C | GRCh38 |
| NC_000013.10:g.48619763T>C , CM000675.1:g.48619763T>C | GRCh37 |
| NC_000013.9:g.47517764T>C | NCBI36 |
| NG_047021.1:g.13061T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000258662.3:c.356-33T>C MANE Select | ENSP00000258662.1:n.356-33T>C | |
| ENST00000258662.2:c.356-33T>C | ENSP00000258662.1:n.356-33T>C | |
| NM_018283.2:c.356-33T>C | NP_060753.1:n.356-33T>C | |
| NM_018283.3:c.356-33T>C | NP_060753.1:n.356-33T>C | |
| NR_136687.1:n.536-33T>C | ||
| NR_136688.1:n.536-33T>C | ||
| NM_018283.4:c.356-33T>C MANE Select | NP_060753.1:n.356-33T>C | |
| NR_136687.2:n.377-33T>C | ||
| NR_136688.2:n.377-33T>C |