HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992812_177992813delinsTC , CM000667.2:g.177992812_177992813delinsTC | GRCh38 |
NC_000005.9:g.177419813_177419814delinsTC , CM000667.1:g.177419813_177419814delinsTC | GRCh37 |
NC_000005.8:g.177352419_177352420delinsTC | NCBI36 |
NG_015889.1:g.8430_8431delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.577_578delinsGA MANE Select | ENSP00000311290.2:p.Asp193= | |
NM_006261.4:c.577_578delinsGA | NP_006252.3:p.Asp193= | |
NM_006261.5:c.577_578delinsGA MANE Select | NP_006252.4:p.Asp193= |