Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31535413G>T , CM000680.2:g.31535413G>T | GRCh38 |
| NC_000018.9:g.29115376G>T , CM000680.1:g.29115376G>T | GRCh37 |
| NC_000018.8:g.27369374G>T | NCBI36 |
| NG_007072.3:g.42172G>T , LRG_397:g.42172G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001943.5:c.1423+1G>T MANE Select | NP_001934.2:n.1423+1G>T |
| ENST00000261590.13:c.1423+1G>T MANE Select | ENSP00000261590.8:n.1423+1G>T |
| NM_001943.3:c.1423+1G>T , LRG_397t1:c.1423+1G>T | NP_001934.2:n.1423+1G>T |
| NM_001943.4:c.1423+1G>T | NP_001934.2:n.1423+1G>T |
| ENST00000261590.12:c.1423+1G>T | ENSP00000261590.8:n.1423+1G>T |
| XM_024451095.1:c.889+1G>T | XP_024306863.1:n.889+1G>T |