dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.49989311C>A , CM000675.2:g.49989311C>A | GRCh38 |
| NC_000013.10:g.50563447C>A , CM000675.1:g.50563447C>A | GRCh37 |
| NC_000013.9:g.49461448C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_002612.1:n.1530-690G>T (DLEU2) | ||
| XM_011535166.1:c.223-690G>T (SPRYD7) | XP_011533468.1:n.223-690G>T | |
| XM_011535167.1:c.223-690G>T (SPRYD7) | XP_011533469.1:n.223-690G>T | |
| NR_152566.1:n.1830-690G>T (DLEU2) |