HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21007301A>T , CM000664.2:g.21007301A>T | GRCh38 |
NC_000002.11:g.21230173A>T , CM000664.1:g.21230173A>T | GRCh37 |
NC_000002.10:g.21083678A>T | NCBI36 |
NG_011793.1:g.41773T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000233242.5:c.9567T>A MANE Select | ENSP00000233242.1:p.Pro3189= | |
ENST00000616098.4:c.9567T>A | ENSP00000477990.1:p.Pro3189= | |
NM_000384.2:c.9567T>A | NP_000375.2:p.Pro3189= | |
XM_011532809.1:c.5869+3432T>A | XP_011531111.1:n.5869+3432T>A | |
NM_000384.3:c.9567T>A MANE Select | NP_000375.3:p.Pro3189= |