dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113072573G>C , CM000664.2:g.113072573G>C | GRCh38 |
| NC_000002.11:g.113830150G>C , CM000664.1:g.113830150G>C | GRCh37 |
| NC_000002.10:g.113546621G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393197.3:c.-166G>C | ENSP00000376893.2:n.-166G>C | |
| ENST00000341010.6:c.-28-138G>C MANE Select | ENSP00000341794.2:n.-28-138G>C | |
| ENST00000393197.2:c.-166G>C | ENSP00000376893.2:n.-166G>C | |
| NM_032556.5:c.-166G>C | NP_115945.4:n.-166G>C | |
| NM_173161.2:c.-28-138G>C | NP_775184.1:n.-28-138G>C | |
| NM_032556.6:c.-166G>C | NP_115945.4:n.-166G>C | |
| NM_173161.3:c.-28-138G>C MANE Select | NP_775184.1:n.-28-138G>C |