HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256056C>G , CM000671.2:g.133256056C>G | GRCh38 |
NC_000009.11:g.136131443C>G , CM000671.1:g.136131443C>G | GRCh37 |
NC_000009.10:g.135121264C>G | NCBI36 |
NG_006669.1:g.21612G>C | |
NG_006669.2:g.24160G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.704G>C | ||
ENST00000647353.1:n.54-4904G>C | ||
ENST00000679909.1:c.28+19106G>C | ENSP00000506089.1:n.28+19106G>C | |
ENST00000453660.3:n.686G>C | ||
ENST00000538324.2:c.672G>C | ENSP00000483018.1:p.Leu224= | |
ENST00000611156.4:c.672G>C | ENSP00000483265.1:p.Leu224= | |
NM_020469.2:c.675G>C | NP_065202.2:p.Leu225= | |
NM_020469.3:c.675G>C | NP_065202.2:p.Leu225= |