HGVS | Genome Assembly |
---|---|
NC_000002.12:g.61378298_61378303del , CM000664.2:g.61378298_61378303del | GRCh38 |
NC_000002.11:g.61605433_61605438del , CM000664.1:g.61605433_61605438del | GRCh37 |
NC_000002.10:g.61458937_61458942del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398571.7:c.1076+60_1076+65del MANE Select | ENSP00000381577.2:n.1076+60_1076+65del | |
ENST00000398571.6:c.1076+60_1076+65del | ENSP00000381577.2:n.1076+60_1076+65del | |
ENST00000453133.1:c.602+60_602+65del | ||
NM_014709.3:c.1076+60_1076+65del | NP_055524.3:n.1076+60_1076+65del | |
NM_014709.4:c.1076+60_1076+65del MANE Select | NP_055524.3:n.1076+60_1076+65del |