HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008460G>T , CM000666.2:g.88008460G>T | GRCh38 |
NC_000004.11:g.88929612G>T , CM000666.1:g.88929612G>T | GRCh37 |
NC_000004.10:g.89148636G>T | NCBI36 |
NG_008604.1:g.5793G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.595+132G>T MANE Select | ENSP00000237596.2:n.595+132G>T | |
ENST00000237596.6:c.595+132G>T | ENSP00000237596.2:n.595+132G>T | |
ENST00000506727.1:n.97+132G>T | ||
NM_000297.3:c.595+132G>T | NP_000288.1:n.595+132G>T | |
XM_011532028.1:c.595+132G>T | XP_011530330.1:n.595+132G>T | |
XR_244632.2:n.690+132G>T | ||
NR_156488.1:n.682+132G>T | ||
XM_011532028.2:c.595+132G>T | XP_011530330.1:n.595+132G>T | |
NM_000297.4:c.595+132G>T MANE Select | NP_000288.1:n.595+132G>T | |
NR_156488.2:n.694+132G>T |