HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94415181G= , CM000669.2:g.94415181G= | GRCh38 |
NC_000007.13:g.94044493G= , CM000669.1:g.94044493G= | GRCh37 |
NC_000007.12:g.93882429G= | NCBI36 |
NG_007405.1:g.25621G= , LRG_2:g.25621G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.1720-45G= MANE Select | ENSP00000297268.6:n.1720-45G= | |
ENST00000297268.10:c.1720-45G= | ENSP00000297268.6:n.1720-45G= | |
ENST00000473573.5:n.57-45G= | ||
ENST00000488298.5:n.144-45G= | ||
ENST00000620463.1:c.1714-45G= | ENSP00000477719.1:n.1714-45G= | |
NM_000089.3:c.1720-45G= , LRG_2t1:c.1720-45G= | NP_000080.2:n.1720-45G= | |
NM_000089.4:c.1720-45G= MANE Select | NP_000080.2:n.1720-45G= |