HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154954075_154954076dup , CM000685.2:g.154954075_154954076dup | GRCh38 |
NC_000023.10:g.154182350_154182351dup , CM000685.1:g.154182350_154182351dup | GRCh37 |
NC_000023.9:g.153835544_153835545dup | NCBI36 |
NG_011403.1:g.73649_73650dup | |
NG_011403.2:g.73649_73650dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1753-33_1753-32dup MANE Select | ENSP00000353393.4:n.1753-33_1753-32dup | |
ENST00000647125.1:c.*1629-33_*1629-32dup | ENSP00000496062.1:n.*1629-33_*1629-32dup | |
ENST00000360256.8:c.1753-33_1753-32dup | ENSP00000353393.4:n.1753-33_1753-32dup | |
NM_000132.3:c.1753-33_1753-32dup | NP_000123.1:n.1753-33_1753-32dup | |
XM_011531126.1:c.1648-33_1648-32dup | XP_011529428.1:n.1648-33_1648-32dup | |
NM_000132.4:c.1753-33_1753-32dup MANE Select | NP_000123.1:n.1753-33_1753-32dup |