HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739626_86739638dup , CM000670.2:g.86739626_86739638dup | GRCh38 |
NC_000008.10:g.87751854_87751866dup , CM000670.1:g.87751854_87751866dup | GRCh37 |
NC_000008.9:g.87820970_87820982dup | NCBI36 |
NG_016980.1:g.9043_9055dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.211+22_211+34dup MANE Select | ENSP00000316605.5:n.211+22_211+34dup | |
ENST00000681746.1:c.211+22_211+34dup | ENSP00000505959.1:n.211+22_211+34dup | |
ENST00000320005.5:c.211+22_211+34dup | ENSP00000316605.5:n.211+22_211+34dup | |
ENST00000519777.1:n.193+22_193+34dup | ||
NM_019098.4:c.211+22_211+34dup | NP_061971.3:n.211+22_211+34dup | |
NM_019098.5:c.211+22_211+34dup MANE Select | NP_061971.3:n.211+22_211+34dup |