HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128344392G>C , CM000667.2:g.128344392G>C | GRCh38 |
NC_000005.9:g.127680084G>C , CM000667.1:g.127680084G>C | GRCh37 |
NC_000005.8:g.127707983G>C | NCBI36 |
NG_008750.1:g.198652C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262464.9:c.3336C>G MANE Select | ENSP00000262464.4:p.Asn1112Lys | |
ENST00000262464.8:c.3336C>G | ENSP00000262464.4:p.Asn1112Lys | |
ENST00000508053.5:c.3336C>G | ENSP00000424571.1:p.Asn1112Lys | |
ENST00000508989.5:c.3237C>G | ENSP00000425596.1:p.Asn1079Lys | |
ENST00000619499.4:c.3333C>G | ENSP00000482132.1:p.Asn1111Lys | |
NM_001999.3:c.3336C>G | NP_001990.2:p.Asn1112Lys | |
XM_017009228.2:c.3183C>G | XP_016864717.1:p.Asn1061Lys | |
NM_001999.4:c.3336C>G MANE Select | NP_001990.2:p.Asn1112Lys |