HGVS | Genome Assembly |
---|---|
NC_000004.12:g.163324730C>A , CM000666.2:g.163324730C>A | GRCh38 |
NC_000004.11:g.164245882C>A , CM000666.1:g.164245882C>A | GRCh37 |
NC_000004.10:g.164465332C>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000296533.3:c.*573G>T MANE Select | ENSP00000354652.2:n.*573G>T | |
ENST00000296533.2:c.*573G>T | ENSP00000354652.2:n.*573G>T | |
NM_000909.5:c.*573G>T | NP_000900.1:n.*573G>T | |
XM_005263031.2:c.*573G>T | XP_005263088.1:n.*573G>T | |
XM_011532010.1:c.*573G>T | XP_011530312.1:n.*573G>T | |
XM_005263031.4:c.*573G>T | XP_005263088.1:n.*573G>T | |
XM_011532010.3:c.*573G>T | XP_011530312.1:n.*573G>T | |
NM_000909.6:c.*573G>T MANE Select | NP_000900.1:n.*573G>T |