HGVS | Genome Assembly |
---|---|
NC_000009.12:g.77794644_77794645del , CM000671.2:g.77794644_77794645del | GRCh38 |
NC_000009.11:g.80409560_80409561del , CM000671.1:g.80409560_80409561del | GRCh37 |
NC_000009.10:g.79599380_79599381del | NCBI36 |
NG_027904.2:g.241659_241660del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286548.9:c.606-53_606-52del MANE Select | ENSP00000286548.4:n.606-53_606-52del | |
ENST00000286548.8:c.606-53_606-52del | ENSP00000286548.4:n.606-53_606-52del | |
NM_002072.4:c.606-53_606-52del | NP_002063.2:n.606-53_606-52del | |
XM_017014628.2:c.432-53_432-52del | XP_016870117.1:n.432-53_432-52del | |
NM_002072.5:c.606-53_606-52del MANE Select | NP_002063.2:n.606-53_606-52del |