HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101425160C= , CM000671.2:g.101425160C= | GRCh38 |
NC_000009.11:g.104187442C= , CM000671.1:g.104187442C= | GRCh37 |
NC_000009.10:g.103227263C= | NCBI36 |
NG_012387.1:g.15621G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647789.2:c.800-118G= MANE Select | ENSP00000497767.1:n.800-118G= | |
ENST00000648064.1:c.800-118G= | ENSP00000497990.1:n.800-118G= | |
ENST00000648758.1:c.800-118G= | ENSP00000497731.1:n.800-118G= | |
ENST00000649902.1:c.800-118G= | ENSP00000497216.1:n.800-118G= | |
ENST00000374855.8:c.800-118G= | ENSP00000363988.4:n.800-118G= | |
ENST00000616752.1:c.800-118G= | ENSP00000481363.1:n.800-118G= | |
NM_000035.3:c.800-118G= | NP_000026.2:n.800-118G= | |
NM_000035.4:c.800-118G= MANE Select | NP_000026.2:n.800-118G= |