dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33022051A>T , CM000675.2:g.33022051A>T | GRCh38 |
| NC_000013.10:g.33596189A>T , CM000675.1:g.33596189A>T | GRCh37 |
| NC_000013.9:g.32494189A>T | NCBI36 |
| NG_011485.1:g.10619A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.819+4792A>T MANE Select | ENSP00000369442.3:n.819+4792A>T | |
| ENST00000380099.3:c.819+4792A>T | ENSP00000369442.3:n.819+4792A>T | |
| ENST00000487852.1:n.827+4792A>T | ||
| NM_004795.3:c.819+4792A>T | NP_004786.2:n.819+4792A>T | |
| XM_006719895.1:c.-103+5738A>T | XP_006719958.1:n.-103+5738A>T | |
| XM_006719895.2:c.-103+5738A>T | XP_006719958.1:n.-103+5738A>T | |
| NM_004795.4:c.819+4792A>T MANE Select | NP_004786.2:n.819+4792A>T |