HGVS | Genome Assembly |
---|---|
NC_000023.11:g.22032994A>T , CM000685.2:g.22032994A>T | GRCh38 |
NC_000023.10:g.22051112A>T , CM000685.1:g.22051112A>T | GRCh37 |
NC_000023.9:g.21961033A>T | NCBI36 |
NG_007563.2:g.5192A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000475778.2:n.415A>T | ||
ENST00000683214.1:n.415A>T | ||
ENST00000684143.1:c.-12A>T | ENSP00000508264.1:n.-12A>T | |
ENST00000379374.5:c.-12A>T MANE Select | ENSP00000368682.4:n.-12A>T | |
ENST00000379374.4:c.-12A>T | ENSP00000368682.4:n.-12A>T | |
NM_000444.5:c.-12A>T | NP_000435.3:n.-12A>T | |
NM_001282754.1:c.-12A>T | NP_001269683.1:n.-12A>T | |
XM_011545535.1:c.-12A>T | XP_011543837.1:n.-12A>T | |
XR_001755695.1:n.668A>T | ||
NM_000444.6:c.-12A>T MANE Select | NP_000435.3:n.-12A>T | |
NM_001282754.2:c.-12A>T | NP_001269683.1:n.-12A>T |