HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117835439C>T , CM000670.2:g.117835439C>T | GRCh38 |
NC_000008.10:g.118847678C>T , CM000670.1:g.118847678C>T | GRCh37 |
NC_000008.9:g.118916859C>T | NCBI36 |
NG_007455.2:g.281381G>A , LRG_493:g.281381G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.631+5G>A | ||
ENST00000378204.7:c.1164+5G>A MANE Select | ENSP00000367446.3:n.1164+5G>A | |
ENST00000436216.2:c.532+5G>A | ||
ENST00000378204.6:c.1164+5G>A | ENSP00000367446.2:n.1164+5G>A | |
ENST00000436216.1:c.532+5G>A | ||
ENST00000437196.1:c.*55+5G>A | ENSP00000407299.1:n.*55+5G>A | |
NM_000127.2:c.1164+5G>A , LRG_493t1:c.1164+5G>A | NP_000118.2:n.1164+5G>A | |
NM_000127.3:c.1164+5G>A MANE Select | NP_000118.2:n.1164+5G>A |