HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96416142A>T , CM000667.2:g.96416142A>T | GRCh38 |
NC_000005.9:g.95751846A>T , CM000667.1:g.95751846A>T | GRCh37 |
NC_000005.8:g.95777602A>T | NCBI36 |
NG_021161.1:g.22140T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.621-21T>A MANE Select | ENSP00000308024.2:n.621-21T>A | |
ENST00000311106.7:c.621-21T>A | ENSP00000308024.2:n.621-21T>A | |
ENST00000508626.5:c.480-21T>A | ENSP00000421600.1:n.480-21T>A | |
NM_000439.4:c.621-21T>A | NP_000430.3:n.621-21T>A | |
NM_001177875.1:c.480-21T>A | NP_001171346.1:n.480-21T>A | |
NR_130776.1:n.354+36490A>T | ||
NM_000439.5:c.621-21T>A MANE Select | NP_000430.3:n.621-21T>A | |
NM_001177875.2:c.480-21T>A | NP_001171346.1:n.480-21T>A |