Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.63322631C>A , CM000663.2:g.63322631C>A | GRCh38 |
| NC_000001.10:g.63788302C>A , CM000663.1:g.63788302C>A | GRCh37 |
| NC_000001.9:g.63560890C>A | NCBI36 |
| NG_012220.1:g.4573C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371116.4:c.-428C>A (FOXD3) MANE Select | ENSP00000360157.2:n.-428C>A | |
| NR_121636.1:n.185+860G>T (FOXD3-AS1) | ||
| NR_121637.1:n.88-1168G>T (FOXD3-AS1) | ||
| NM_012183.3:c.-428C>A (FOXD3) MANE Select | NP_036315.1:n.-428C>A |