HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978277G>T , CM000667.2:g.149978277G>T | GRCh38 |
NC_000005.9:g.149357840G>T , CM000667.1:g.149357840G>T | GRCh37 |
NC_000005.8:g.149338033G>T | NCBI36 |
NG_007147.2:g.19395G>T , LRG_684:g.19395G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.857G>T | ||
ENST00000286298.5:c.625G>T MANE Select | ENSP00000286298.4:p.Asp209Tyr | |
ENST00000286298.4:c.625G>T | ENSP00000286298.4:p.Asp209Tyr | |
ENST00000503336.1:c.298G>T | ENSP00000426053.1:p.Asp100Tyr | |
NM_000112.3:c.625G>T , LRG_684t1:c.625G>T | NP_000103.2:p.Asp209Tyr | |
XM_017009191.2:c.625G>T | XP_016864680.1:p.Asp209Tyr | |
NM_000112.4:c.625G>T MANE Select | NP_000103.2:p.Asp209Tyr |