HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88427344G>T , CM000678.2:g.88427344G>T | GRCh38 |
NC_000016.9:g.88493752G>T , CM000678.1:g.88493752G>T | GRCh37 |
NC_000016.8:g.87021253G>T | NCBI36 |
NG_012236.2:g.4874G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000565624.3:c.-126-1G>T MANE Select | ENSP00000456500.2:n.-126-1G>T | |
XM_011523386.1:c.-126-1G>T | XP_011521688.1:n.-126-1G>T | |
XM_011523387.1:c.-126-1G>T | XP_011521689.1:n.-126-1G>T | |
XM_011523388.1:c.-126-1G>T | XP_011521690.1:n.-126-1G>T | |
XM_017023784.1:c.-127G>T | XP_016879273.1:n.-127G>T | |
XM_017023785.1:c.-126-1G>T | XP_016879274.1:n.-126-1G>T | |
XR_002957934.1:n.250+2620C>A | ||
NM_001367624.2:c.-126-1G>T MANE Select | NP_001354553.1:n.-126-1G>T |