HGVS | Genome Assembly |
---|---|
NC_000003.12:g.139460011T>A , CM000665.2:g.139460011T>A | GRCh38 |
NC_000003.11:g.139178853T>A , CM000665.1:g.139178853T>A | GRCh37 |
NC_000003.10:g.140661543T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000232217.6:c.252+2101A>T (RBP2) MANE Select | ENSP00000232217.2:n.252+2101A>T | |
ENST00000511956.1:c.252+2101A>T (RBP2) | ENSP00000424333.1:n.252+2101A>T | |
NM_004164.2:c.252+2101A>T (RBP2) | NP_004155.2:n.252+2101A>T | |
NR_121609.1:n.354+36897T>A (COPB2-DT) | ||
NM_004164.3:c.252+2101A>T (RBP2) MANE Select | NP_004155.2:n.252+2101A>T |