HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154896262_154896265del , CM000685.2:g.154896262_154896265del | GRCh38 |
NC_000023.10:g.154124537_154124540del , CM000685.1:g.154124537_154124540del | GRCh37 |
NC_000023.9:g.153777731_153777734del | NCBI36 |
NG_011403.1:g.131460_131463del | |
NG_011403.2:g.131460_131463del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6274-32_6274-29del MANE Select | ENSP00000353393.4:n.6274-32_6274-29del | |
ENST00000360256.8:c.6274-32_6274-29del | ENSP00000353393.4:n.6274-32_6274-29del | |
NM_000132.3:c.6274-32_6274-29del | NP_000123.1:n.6274-32_6274-29del | |
XM_011531126.1:c.6169-32_6169-29del | XP_011529428.1:n.6169-32_6169-29del | |
NM_000132.4:c.6274-32_6274-29del MANE Select | NP_000123.1:n.6274-32_6274-29del |