HGVS | Genome Assembly |
---|---|
NC_000020.11:g.45948023A>C , CM000682.2:g.45948023A>C | GRCh38 |
NC_000020.10:g.44576662A>C , CM000682.1:g.44576662A>C | GRCh37 |
NC_000020.9:g.44010069A>C | NCBI36 |
NG_029772.1:g.29172T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372409.7:c.*268A>C | ENSP00000361486.3:n.*268A>C | |
ENST00000479348.2:c.1324A>C | ||
NM_022104.3:c.*268A>C | NP_071387.1:n.*268A>C | |
XM_011528980.1:c.*268A>C | XP_011527282.1:n.*268A>C | |
XM_011528981.1:c.*268A>C | XP_011527283.1:n.*268A>C | |
XM_011528982.1:c.*268A>C | XP_011527284.1:n.*268A>C | |
XM_017028014.2:c.*268A>C | XP_016883503.1:n.*268A>C |