HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135832883_135832891del , CM000664.2:g.135832883_135832891del | GRCh38 |
NC_000002.11:g.136590453_136590461del , CM000664.1:g.136590453_136590461del | GRCh37 |
NC_000002.10:g.136306923_136306931del | NCBI36 |
NG_008104.2:g.27281_27289del , LRG_338:g.27281_27289del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.720+222_720+230del MANE Select | ENSP00000264162.2:n.720+222_720+230del | |
ENST00000264162.6:c.720+222_720+230del | ENSP00000264162.2:n.720+222_720+230del | |
NM_002299.2:c.720+222_720+230del , LRG_338t1:c.720+222_720+230del | NP_002290.2:n.720+222_720+230del | |
NM_002299.3:c.720+222_720+230del | NP_002290.2:n.720+222_720+230del | |
XM_017004088.2:c.720+222_720+230del | XP_016859577.1:n.720+222_720+230del | |
NM_002299.4:c.720+222_720+230del MANE Select | NP_002290.2:n.720+222_720+230del |