HGVS | Genome Assembly |
---|---|
NC_000004.12:g.163324714G>T , CM000666.2:g.163324714G>T | GRCh38 |
NC_000004.11:g.164245866G>T , CM000666.1:g.164245866G>T | GRCh37 |
NC_000004.10:g.164465316G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000296533.3:c.*589C>A MANE Select | ENSP00000354652.2:n.*589C>A | |
ENST00000296533.2:c.*589C>A | ENSP00000354652.2:n.*589C>A | |
NM_000909.5:c.*589C>A | NP_000900.1:n.*589C>A | |
XM_005263031.2:c.*589C>A | XP_005263088.1:n.*589C>A | |
XM_011532010.1:c.*589C>A | XP_011530312.1:n.*589C>A | |
XM_005263031.4:c.*589C>A | XP_005263088.1:n.*589C>A | |
XM_011532010.3:c.*589C>A | XP_011530312.1:n.*589C>A | |
NM_000909.6:c.*589C>A MANE Select | NP_000900.1:n.*589C>A |