HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99352894C>A , CM000666.2:g.99352894C>A | GRCh38 |
NC_000004.11:g.100274051C>A , CM000666.1:g.100274051C>A | GRCh37 |
NC_000004.10:g.100493074C>A | NCBI36 |
NG_011718.1:g.4867G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515683.5:c.-219G>T | ENSP00000426083.1:n.-219G>T | |
NM_000669.4:c.-219G>T | NP_000660.1:n.-219G>T | |
NR_133005.1:n.152G>T | ||
XM_011531588.1:c.-219G>T | XP_011529890.1:n.-219G>T | |
XM_011531589.1:c.-459G>T | XP_011529891.1:n.-459G>T |