HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188913T>G , CM000675.2:g.20188913T>G | GRCh38 |
NC_000013.10:g.20763052T>G , CM000675.1:g.20763052T>G | GRCh37 |
NC_000013.9:g.19661052T>G | NCBI36 |
NG_008358.1:g.9063A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.669A>C | ENSP00000372295.1:p.Lys223Asn | |
ENST00000382848.5:c.669A>C MANE Select | ENSP00000372299.4:p.Lys223Asn | |
ENST00000382844.1:c.669A>C | ENSP00000372295.1:p.Lys223Asn | |
ENST00000382848.4:c.669A>C | ENSP00000372299.4:p.Lys223Asn | |
NM_004004.5:c.669A>C | NP_003995.2:p.Lys223Asn | |
XM_011535049.1:c.669A>C | XP_011533351.1:p.Lys223Asn | |
XM_011535049.2:c.669A>C | XP_011533351.1:p.Lys223Asn | |
NM_004004.6:c.669A>C MANE Select | NP_003995.2:p.Lys223Asn |