Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404259T>C , CM000666.2:g.73404259T>C | GRCh38 |
| NC_000004.11:g.74269976T>C , CM000666.1:g.74269976T>C | GRCh37 |
| NC_000004.10:g.74488840T>C | NCBI36 |
| NG_009291.1:g.5005T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295897.8:c.-69T>C | ENSP00000295897.4:n.-69T>C | |
| ENST00000441319.5:c.48-110T>C | ENSP00000392541.1:n.48-110T>C | |
| ENST00000621628.4:c.-69T>C | ENSP00000480485.1:n.-69T>C | |
| NM_000477.5:c.-69T>C | NP_000468.1:n.-69T>C | |
| NM_000477.6:c.-69T>C | NP_000468.1:n.-69T>C |