HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154953779A>G , CM000685.2:g.154953779A>G | GRCh38 |
NC_000023.10:g.154182054A>G , CM000685.1:g.154182054A>G | GRCh37 |
NC_000023.9:g.153835248A>G | NCBI36 |
NG_011403.1:g.73945T>C | |
NG_011403.2:g.73945T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1903+113T>C MANE Select | ENSP00000353393.4:n.1903+113T>C | |
ENST00000647125.1:c.*1779+113T>C | ENSP00000496062.1:n.*1779+113T>C | |
ENST00000360256.8:c.1903+113T>C | ENSP00000353393.4:n.1903+113T>C | |
NM_000132.3:c.1903+113T>C | NP_000123.1:n.1903+113T>C | |
XM_011531126.1:c.1798+113T>C | XP_011529428.1:n.1798+113T>C | |
NM_000132.4:c.1903+113T>C MANE Select | NP_000123.1:n.1903+113T>C |