HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32474986G>A , CM000684.2:g.32474986G>A | GRCh38 |
NC_000022.10:g.32870973G>A , CM000684.1:g.32870973G>A | GRCh37 |
NC_000022.9:g.31200973G>A | NCBI36 |
NG_016001.1:g.5267G>A | |
NG_016001.2:g.5267G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266087.12:c.-17G>A MANE Select | ENSP00000266087.7:n.-17G>A | |
ENST00000266087.11:c.-17G>A | ENSP00000266087.7:n.-17G>A | |
ENST00000420700.5:c.-17G>A | ENSP00000406155.1:n.-17G>A | |
ENST00000425028.5:c.-17G>A | ENSP00000395823.1:n.-17G>A | |
NM_012179.3:c.-17G>A | NP_036311.3:n.-17G>A | |
XM_011530106.1:c.-190G>A | XP_011528408.1:n.-190G>A | |
XM_024452207.1:c.-207G>A | XP_024307975.1:n.-207G>A | |
NM_012179.4:c.-17G>A MANE Select | NP_036311.3:n.-17G>A |