dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36700882T>G , CM000684.2:g.36700882T>G | GRCh38 |
| NC_000022.10:g.37096927T>G , CM000684.1:g.37096927T>G | GRCh37 |
| NC_000022.9:g.35426873T>G | NCBI36 |
| NG_031861.1:g.6764A>C | |
| NG_031861.2:g.6977A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.211+1484A>C MANE Select | ENSP00000300105.6:n.211+1484A>C | |
| ENST00000300105.6:c.211+1484A>C | ENSP00000300105.6:n.211+1484A>C | |
| NM_006078.3:c.211+1484A>C | NP_006069.1:n.211+1484A>C | |
| NM_006078.4:c.211+1484A>C | NP_006069.1:n.211+1484A>C | |
| NM_001379051.1:c.142+1484A>C | NP_001365980.1:n.142+1484A>C | |
| NM_006078.5:c.211+1484A>C MANE Select | NP_006069.1:n.211+1484A>C | |
| NR_166440.1:n.1387+1484A>C |