HGVS | Genome Assembly |
---|---|
NC_000009.12:g.137199356C>G , CM000671.2:g.137199356C>G | GRCh38 |
NC_000009.11:g.140093808C>G , CM000671.1:g.140093808C>G | GRCh37 |
NC_000009.10:g.139213629C>G | NCBI36 |
NG_027801.1:g.6356G>C | |
NG_027801.2:g.9838G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409012.6:c.1356G>C MANE Select | ENSP00000387100.4:p.Gly452= | |
ENST00000333046.8:c.750G>C | ENSP00000327617.4:p.Gly250= | |
ENST00000409012.4:c.1356G>C | ENSP00000387100.4:p.Gly452= | |
ENST00000541945.1:n.90+4748G>C | ||
NM_001128228.2:c.1356G>C | NP_001121700.2:p.Gly452= | |
NM_001128228.3:c.1356G>C MANE Select | NP_001121700.2:p.Gly452= |