Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29251101G>A , CM000664.2:g.29251101G>A | GRCh38 |
| NC_000002.11:g.29473967G>A , CM000664.1:g.29473967G>A | GRCh37 |
| NC_000002.10:g.29327471G>A | NCBI36 |
| NG_009445.1:g.675466C>T , LRG_488:g.675466C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.2204+4C>T MANE Select | NP_004295.2:n.2204+4C>T |
| ENST00000389048.8:c.2204+4C>T MANE Select | ENSP00000373700.3:n.2204+4C>T |
| NM_004304.4:c.2204+4C>T | NP_004295.2:n.2204+4C>T |
| ENST00000389048.7:c.2204+4C>T | ENSP00000373700.3:n.2204+4C>T |
| ENST00000618119.4:c.1073+4C>T | ENSP00000482733.1:n.1073+4C>T |
| XR_001738688.2:n.3134+4C>T |