HGVS | Genome Assembly |
---|---|
NC_000002.12:g.215064212del , CM000664.2:g.215064212del | GRCh38 |
NC_000002.11:g.215928935del , CM000664.1:g.215928935del | GRCh37 |
NC_000002.10:g.215637180del | NCBI36 |
NG_007074.1:g.79217del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000272895.12:c.171del MANE Select | ENSP00000272895.7:p.Ala58HisfsTer? | |
ENST00000272895.11:c.171del | ENSP00000272895.7:p.Ala58HisfsTer? | |
NM_173076.2:c.171del | NP_775099.2:p.Ala58HisfsTer? | |
NR_103740.1:n.391del | ||
XM_011510951.1:c.171del | XP_011509253.1:p.Ala58HisfsTer? | |
XM_011510952.1:c.171del | XP_011509254.1:p.Ala58HisfsTer? | |
XM_011510951.2:c.171del | XP_011509253.1:p.Ala58HisfsTer? | |
NM_173076.3:c.171del MANE Select | NP_775099.2:p.Ala58HisfsTer? | |
NR_103740.2:n.589del |