HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256099T= , CM000671.2:g.133256099T= | GRCh38 |
NC_000009.11:g.136131486T= , CM000671.1:g.136131486T= | GRCh37 |
NC_000009.10:g.135121307T= | NCBI36 |
NG_006669.1:g.21569A= | |
NG_006669.2:g.24117A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.661A= | ||
ENST00000647353.1:n.54-4947A= | ||
ENST00000679909.1:c.28+19063A= | ENSP00000506089.1:n.28+19063A= | |
ENST00000453660.3:n.643A= | ||
ENST00000538324.2:c.629A= | ENSP00000483018.1:p.Asp210= | |
ENST00000611156.4:c.629A= | ENSP00000483265.1:p.Asp210= | |
NM_020469.2:c.632A= | NP_065202.2:p.Asp211= | |
NM_020469.3:c.632A= | NP_065202.2:p.Asp211= |