Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18399961G>C , CM000670.2:g.18399961G>C | GRCh38 |
| NC_000008.10:g.18257471G>C , CM000670.1:g.18257471G>C | GRCh37 |
| NC_000008.9:g.18301751G>C | NCBI36 |
| NG_012246.1:g.13717G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.-6-37G>C MANE Select | ENSP00000286479.3:n.-6-37G>C | |
| ENST00000286479.3:c.-6-37G>C | ENSP00000286479.3:n.-6-37G>C | |
| ENST00000520116.1:c.-57-376G>C | ENSP00000428416.1:n.-57-376G>C | |
| NM_000015.2:c.-6-37G>C | NP_000006.2:n.-6-37G>C | |
| XM_011544358.1:c.-6-37G>C | XP_011542660.1:n.-6-37G>C | |
| XM_017012938.1:c.-6-37G>C | XP_016868427.1:n.-6-37G>C | |
| NM_000015.3:c.-6-37G>C MANE Select | NP_000006.2:n.-6-37G>C |