HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17023973C= , CM000663.2:g.17023973C= | GRCh38 |
NC_000001.10:g.17350468C= , CM000663.1:g.17350468C= | GRCh37 |
NC_000001.9:g.17223055C= | NCBI36 |
NG_012340.1:g.35198G= , LRG_316:g.35198G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.471G= | ENSP00000481376.2:p.Gln157= | |
ENST00000491274.6:c.600G= | ENSP00000480482.2:p.Gln200= | |
ENST00000375499.8:c.642G= MANE Select | ENSP00000364649.3:p.Gln214= | |
ENST00000375499.7:c.642G= | ENSP00000364649.3:p.Gln214= | |
ENST00000485515.5:n.576G= | ||
ENST00000491274.5:c.600G= | ENSP00000480482.1:p.Gln200= | |
NM_003000.2:c.642G= , LRG_316t1:c.642G= | NP_002991.2:p.Gln214= | |
NM_003000.3:c.642G= MANE Select | NP_002991.2:p.Gln214= |