HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48474272T>C , CM000677.2:g.48474272T>C | GRCh38 |
NC_000015.9:g.48766469T>C , CM000677.1:g.48766469T>C | GRCh37 |
NC_000015.8:g.46553761T>C | NCBI36 |
NG_008805.2:g.176517A>G , LRG_778:g.176517A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4193A>G | ENSP00000453958.2:p.Asp1398Gly | |
ENST00000674301.2:c.4193A>G | ENSP00000501333.2:p.Asp1398Gly | |
ENST00000684448.1:n.2867A>G | ||
ENST00000316623.10:c.4193A>G MANE Select | ENSP00000325527.5:p.Asp1398Gly | |
ENST00000316623.9:c.4193A>G | ENSP00000325527.5:p.Asp1398Gly | |
ENST00000537463.6:c.865A>G | ENSP00000440294.2:p.Met289Val | |
NM_000138.4:c.4193A>G , LRG_778t1:c.4193A>G | NP_000129.3:p.Asp1398Gly | |
NM_000138.5:c.4193A>G MANE Select | NP_000129.3:p.Asp1398Gly |