HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1415313G= , CM000667.2:g.1415313G= | GRCh38 |
NC_000005.9:g.1415428G= , CM000667.1:g.1415428G= | GRCh37 |
NC_000005.8:g.1468428G= | NCBI36 |
NG_015885.1:g.35116C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1032-498C= MANE Select | ENSP00000270349.9:n.1032-498C= | |
ENST00000270349.11:c.1032-498C= | ENSP00000270349.9:n.1032-498C= | |
ENST00000511750.1:n.482-498C= | ||
NM_001044.4:c.1032-498C= | NP_001035.1:n.1032-498C= | |
NM_001044.5:c.1032-498C= MANE Select | NP_001035.1:n.1032-498C= |