HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782696G>C , CM000663.2:g.58782696G>C | GRCh38 |
NC_000001.10:g.59248368G>C , CM000663.1:g.59248368G>C | GRCh37 |
NC_000001.9:g.59020956G>C | NCBI36 |
NG_047027.1:g.6418C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.441C>G | ENSP00000518166.1:p.Asn147Lys | |
ENST00000371222.4:c.375C>G MANE Select | ENSP00000360266.2:p.Asn125Lys | |
ENST00000678696.1:c.375C>G | ENSP00000503132.1:p.Asn125Lys | |
ENST00000371222.3:c.375C>G | ENSP00000360266.2:p.Asn125Lys | |
NM_002228.3:c.375C>G | NP_002219.1:p.Asn125Lys | |
NM_002228.4:c.375C>G MANE Select | NP_002219.1:p.Asn125Lys |