Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624235T>C , CM000679.2:g.41624235T>C | GRCh38 |
| NC_000017.10:g.39780487T>C , CM000679.1:g.39780487T>C | GRCh37 |
| NC_000017.9:g.37034013T>C | NCBI36 |
| NG_008625.1:g.5396A>G | |
| NG_009090.2:g.167478A>G , LRG_401:g.167478A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.275A>G MANE Select | ENSP00000308452.8:p.Asn92Ser | |
| ENST00000311208.12:c.275A>G | ENSP00000308452.8:p.Asn92Ser | |
| ENST00000463128.5:c.-312-29A>G | ENSP00000468672.1:n.-312-29A>G | |
| ENST00000491673.1:n.341A>G | ||
| ENST00000493253.5:n.62A>G | ||
| ENST00000540235.5:c.70A>G | ENSP00000441751.2:p.Met24Val | |
| ENST00000577817.3:c.230A>G | ENSP00000467418.1:p.Asn77Ser | |
| NM_000422.2:c.275A>G | NP_000413.1:p.Asn92Ser | |
| NM_000422.3:c.275A>G MANE Select | NP_000413.1:p.Asn92Ser |