gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.38595658G>A , CM000667.2:g.38595658G>A | GRCh38 |
| NC_000005.9:g.38595760G>A , CM000667.1:g.38595760G>A | GRCh37 |
| NC_000005.8:g.38631517G>A | NCBI36 |
| NG_011817.1:g.4748C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507786.1:n.306-275C>T (LIFR) | ||
| NR_103553.1:n.2540+589G>A (LIFR-AS1) | ||
| NR_103554.1:n.2540+589G>A (LIFR-AS1) | ||
| XM_017009463.1:c.-142-275C>T (LIFR) | XP_016864952.1:n.-142-275C>T |