Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.38594967T>A , CM000667.2:g.38594967T>A | GRCh38 |
| NC_000005.9:g.38595069T>A , CM000667.1:g.38595069T>A | GRCh37 |
| NC_000005.8:g.38630826T>A | NCBI36 |
| NG_011817.1:g.5439A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263409.8:c.-20+294A>T (LIFR) | ENSP00000263409.4:n.-20+294A>T | |
| ENST00000503088.1:n.144+294A>T (LIFR) | ||
| NM_002310.5:c.-20+294A>T (LIFR) | NP_002301.1:n.-20+294A>T | |
| NR_103553.1:n.2438T>A (LIFR-AS1) | ||
| NR_103554.1:n.2438T>A (LIFR-AS1) | ||
| XM_017009462.1:c.-104A>T (LIFR) | XP_016864951.1:n.-104A>T | |
| XM_017009463.1:c.-20+294A>T (LIFR) | XP_016864952.1:n.-20+294A>T | |
| NM_002310.6:c.-20+294A>T (LIFR) | NP_002301.1:n.-20+294A>T |