Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8732046T>G , CM000685.2:g.8732046T>G | GRCh38 |
| NC_000023.10:g.8700087T>G , CM000685.1:g.8700087T>G | GRCh37 |
| NC_000023.9:g.8660087T>G | NCBI36 |
| NG_007088.1:g.5141A>C | |
| NG_007088.2:g.5141A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.-10A>C MANE Select | ENSP00000262648.3:n.-10A>C | |
| ENST00000262648.7:c.-10A>C | ENSP00000262648.3:n.-10A>C | |
| ENST00000619786.1:c.-10A>C | ENSP00000478734.1:n.-10A>C | |
| NM_000216.2:c.-10A>C | NP_000207.2:n.-10A>C | |
| XM_005274501.3:c.-10A>C | XP_005274558.1:n.-10A>C | |
| NM_000216.3:c.-10A>C | NP_000207.2:n.-10A>C | |
| XM_005274501.4:c.-10A>C | XP_005274558.1:n.-10A>C | |
| NM_000216.4:c.-10A>C MANE Select | NP_000207.2:n.-10A>C |