HGVS | Genome Assembly |
---|---|
NC_000006.12:g.159981673G>A , CM000668.2:g.159981673G>A | GRCh38 |
NC_000006.11:g.160402705G>A , CM000668.1:g.160402705G>A | GRCh37 |
NC_000006.10:g.160322695G>A | NCBI36 |
NG_011785.3:g.17575G>A | |
NG_011785.4:g.17575G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356956.6:c.150-9511G>A MANE Select | ENSP00000349437.1:n.150-9511G>A | |
ENST00000676781.1:c.150-9511G>A | ENSP00000504419.1:n.150-9511G>A | |
ENST00000677704.1:c.150-9511G>A | ENSP00000503314.1:n.150-9511G>A | |
ENST00000356956.5:c.150-9511G>A | ENSP00000349437.1:n.150-9511G>A | |
NM_000876.2:c.150-9511G>A | NP_000867.2:n.150-9511G>A | |
XR_942419.1:n.165-9511G>A | ||
NM_000876.3:c.150-9511G>A | NP_000867.2:n.150-9511G>A | |
NM_000876.4:c.150-9511G>A MANE Select | NP_000867.3:n.150-9511G>A |