HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48508619A>T , CM000677.2:g.48508619A>T | GRCh38 |
NC_000015.9:g.48800816A>T , CM000677.1:g.48800816A>T | GRCh37 |
NC_000015.8:g.46588108A>T | NCBI36 |
NG_008805.2:g.142170T>A , LRG_778:g.142170T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.1800T>A | ENSP00000453958.2:p.Pro600= | |
ENST00000674301.2:c.1800T>A | ENSP00000501333.2:p.Pro600= | |
ENST00000684448.1:n.474T>A | ||
ENST00000316623.10:c.1800T>A MANE Select | ENSP00000325527.5:p.Pro600= | |
ENST00000316623.9:c.1800T>A | ENSP00000325527.5:p.Pro600= | |
ENST00000537463.6:c.636+29092T>A | ENSP00000440294.2:n.636+29092T>A | |
NM_000138.4:c.1800T>A , LRG_778t1:c.1800T>A | NP_000129.3:p.Pro600= | |
NM_000138.5:c.1800T>A MANE Select | NP_000129.3:p.Pro600= |