Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21854349A>G , CM000669.2:g.21854349A>G | GRCh38 |
| NC_000007.13:g.21893967A>G , CM000669.1:g.21893967A>G | GRCh37 |
| NC_000007.12:g.21860492A>G | NCBI36 |
| NG_012886.2:g.316135A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.11096A>G MANE Select | NP_001264044.1:p.Asn3699Ser |
| ENST00000409508.8:c.11096A>G MANE Select | ENSP00000475939.1:p.Asn3699Ser |
| NM_001277115.1:c.11096A>G | NP_001264044.1:p.Asn3699Ser |
| ENST00000328843.10:c.11117A>G | ENSP00000330671.7:p.Asn3706Ser |
| ENST00000409508.7:c.11096A>G | ENSP00000475939.1:p.Asn3699Ser |
| ENST00000421290.1:n.279A>G | |
| ENST00000607413.5:n.359A>G | |
| ENST00000620169.4:c.11117A>G | ENSP00000481693.1:p.Asn3706Ser |