HGVS | Genome Assembly |
---|---|
NC_000002.12:g.61378485_61378505del , CM000664.2:g.61378485_61378505del | GRCh38 |
NC_000002.11:g.61605620_61605640del , CM000664.1:g.61605620_61605640del | GRCh37 |
NC_000002.10:g.61459124_61459144del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398571.7:c.1015-81_1015-61del MANE Select | ENSP00000381577.2:n.1015-81_1015-61del | |
ENST00000398571.6:c.1015-81_1015-61del | ENSP00000381577.2:n.1015-81_1015-61del | |
ENST00000453133.1:c.541-81_541-61del | ||
NM_014709.3:c.1015-81_1015-61del | NP_055524.3:n.1015-81_1015-61del | |
NM_014709.4:c.1015-81_1015-61del MANE Select | NP_055524.3:n.1015-81_1015-61del |