HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154905011T>C , CM000685.2:g.154905011T>C | GRCh38 |
NC_000023.10:g.154133286T>C , CM000685.1:g.154133286T>C | GRCh37 |
NC_000023.9:g.153786480T>C | NCBI36 |
NG_011403.1:g.122713A>G | |
NG_011403.2:g.122713A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5386A>G MANE Select | ENSP00000353393.4:p.Asn1796Asp | |
ENST00000360256.8:c.5386A>G | ENSP00000353393.4:p.Asn1796Asp | |
NM_000132.3:c.5386A>G | NP_000123.1:p.Asn1796Asp | |
XM_011531126.1:c.5281A>G | XP_011529428.1:p.Asn1761Asp | |
NM_000132.4:c.5386A>G MANE Select | NP_000123.1:p.Asn1796Asp |