HGVS | Genome Assembly |
---|---|
NC_000009.12:g.841697_841708del , CM000671.2:g.841697_841708del | GRCh38 |
NC_000009.11:g.841697_841708del , CM000671.1:g.841697_841708del | GRCh37 |
NC_000009.10:g.831697_831708del | NCBI36 |
NG_009221.1:g.5008_5019del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382276.8:c.-142_-131del MANE Select | ENSP00000371711.3:n.-142_-131del | |
ENST00000382276.7:c.-142_-131del | ENSP00000371711.3:n.-142_-131del | |
ENST00000564322.1:n.8_19del | ||
NM_021951.2:c.-142_-131del | NP_068770.2:n.-142_-131del | |
XM_006716732.1:c.-142_-131del | XP_006716795.1:n.-142_-131del | |
XM_017014375.1:c.-142_-131del | XP_016869864.1:n.-142_-131del | |
NM_021951.3:c.-142_-131del MANE Select | NP_068770.2:n.-142_-131del |