HGVS | Genome Assembly |
---|---|
NC_000002.12:g.74145294G>C , CM000664.2:g.74145294G>C | GRCh38 |
NC_000002.11:g.74372421G>C , CM000664.1:g.74372421G>C | GRCh37 |
NC_000002.10:g.74225929G>C | NCBI36 |
NG_031910.1:g.7619C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327428.10:c.64C>G MANE Select | ENSP00000331369.5:p.His22Asp | |
ENST00000295326.4:c.64C>G | ENSP00000295326.4:p.His22Asp | |
ENST00000327428.9:c.64C>G | ENSP00000331369.5:p.His22Asp | |
ENST00000469676.1:n.1087C>G | ||
ENST00000477685.5:n.215C>G | ||
ENST00000484655.1:n.2619C>G | ||
NM_001035505.1:c.64C>G | NP_001030582.1:p.His22Asp | |
NM_212552.2:c.64C>G | NP_997717.2:p.His22Asp | |
NM_212552.3:c.64C>G MANE Select | NP_997717.2:p.His22Asp | |
NM_001035505.2:c.64C>G | NP_001030582.1:p.His22Asp |