HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183207900G>C , CM000663.2:g.183207900G>C | GRCh38 |
NC_000001.10:g.183177035G>C , CM000663.1:g.183177035G>C | GRCh37 |
NC_000001.9:g.181443658G>C | NCBI36 |
NG_007079.2:g.26637G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264144.5:c.99G>C MANE Select | ENSP00000264144.4:p.Lys33Asn | |
ENST00000264144.4:c.99G>C | ENSP00000264144.4:p.Lys33Asn | |
ENST00000493293.5:c.99G>C | ENSP00000432063.1:p.Lys33Asn | |
NM_005562.2:c.99G>C | NP_005553.2:p.Lys33Asn | |
NM_018891.2:c.99G>C | NP_061486.2:p.Lys33Asn | |
XM_017001273.2:c.99G>C | XP_016856762.1:p.Lys33Asn | |
NM_005562.3:c.99G>C MANE Select | NP_005553.2:p.Lys33Asn | |
NM_018891.3:c.99G>C | NP_061486.2:p.Lys33Asn |