Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.69187449A>C , CM000678.2:g.69187449A>C | GRCh38 |
| NC_000016.9:g.69221352A>C , CM000678.1:g.69221352A>C | GRCh37 |
| NC_000016.8:g.67778853A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336278.9:c.283A>C (SNTB2) MANE Select | ENSP00000338191.4:p.Ser95Arg | |
| ENST00000336278.8:c.283A>C (SNTB2) | ENSP00000338191.4:p.Ser95Arg | |
| ENST00000467311.5:c.283A>C (SNTB2) | ENSP00000436443.1:p.Ser95Arg | |
| ENST00000567287.2:n.82+20264A>C (UTP4) | ||
| NM_006750.3:c.283A>C (SNTB2) | NP_006741.1:p.Ser95Arg | |
| NM_006750.4:c.283A>C (SNTB2) MANE Select | NP_006741.1:p.Ser95Arg | |
| NR_172088.1:n.286A>C (SNTB2) | ||
| NR_172089.1:n.286A>C (SNTB2) | ||
| NR_172090.1:n.286A>C (SNTB2) |