HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877423_240877424del , CM000664.2:g.240877423_240877424del | GRCh38 |
NC_000002.11:g.241816840_241816841del , CM000664.1:g.241816840_241816841del | GRCh37 |
NC_000002.10:g.241465513_241465514del | NCBI36 |
NG_008005.1:g.13679_13680del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.847-114_847-113del MANE Select | ENSP00000302620.3:n.847-114_847-113del | |
ENST00000307503.3:c.847-114_847-113del | ENSP00000302620.3:n.847-114_847-113del | |
ENST00000470255.1:n.511_512del | ||
NM_000030.2:c.847-114_847-113del | NP_000021.1:n.847-114_847-113del | |
NM_000030.3:c.847-114_847-113del MANE Select | NP_000021.1:n.847-114_847-113del |