HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813832_129813833del , CM000671.2:g.129813832_129813833del | GRCh38 |
NC_000009.11:g.132576111_132576112del , CM000671.1:g.132576111_132576112del | GRCh37 |
NC_000009.10:g.131615932_131615933del | NCBI36 |
NG_008049.1:g.15331_15332del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*140_*141del MANE Select | ENSP00000345719.4:n.*140_*141del | |
ENST00000651202.1:c.*407_*408del | ENSP00000498222.1:n.*407_*408del | |
ENST00000351698.4:c.*140_*141del | ENSP00000345719.4:n.*140_*141del | |
ENST00000474192.1:n.723_724del | ||
NM_000113.2:c.*140_*141del | NP_000104.1:n.*140_*141del | |
XR_929731.3:n.1334_1335del | ||
NM_000113.3:c.*140_*141del MANE Select | NP_000104.1:n.*140_*141del |