HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153770351G>C , CM000685.2:g.153770351G>C | GRCh38 |
NC_000023.10:g.153035806G>C , CM000685.1:g.153035806G>C | GRCh37 |
NC_000023.9:g.152689000G>C | NCBI36 |
NG_013255.1:g.11156G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361971.10:c.1800G>C MANE Select | ENSP00000355378.5:p.Val600= | |
ENST00000361971.9:c.1800G>C | ENSP00000355378.5:p.Val600= | |
ENST00000538966.5:c.1869G>C | ENSP00000442736.1:p.Val623= | |
NM_001163257.1:c.1869G>C | NP_001156729.1:p.Val623= | |
NM_005393.2:c.1800G>C | NP_005384.2:p.Val600= | |
NM_005393.3:c.1800G>C MANE Select | NP_005384.2:p.Val600= | |
NM_001163257.2:c.1869G>C | NP_001156729.1:p.Val623= |