HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667587_31667588dup , CM000683.2:g.31667587_31667588dup | GRCh38 |
NC_000021.8:g.33039900_33039901dup , CM000683.1:g.33039900_33039901dup | GRCh37 |
NC_000021.7:g.31961771_31961772dup | NCBI36 |
NG_008689.1:g.12966_12967dup , LRG_652:g.12966_12967dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.357+212_357+213dup MANE Select | ENSP00000270142.7:n.357+212_357+213dup | |
ENST00000270142.10:c.357+212_357+213dup | ENSP00000270142.6:n.357+212_357+213dup | |
ENST00000389995.4:c.300+212_300+213dup | ENSP00000374645.4:n.300+212_300+213dup | |
ENST00000470944.1:n.1285+212_1285+213dup | ||
NM_000454.4:c.357+212_357+213dup , LRG_652t1:c.357+212_357+213dup | NP_000445.1:n.357+212_357+213dup | |
NM_000454.5:c.357+212_357+213dup MANE Select | NP_000445.1:n.357+212_357+213dup |