HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94409323G>C , CM000669.2:g.94409323G>C | GRCh38 |
NC_000007.13:g.94038635G>C , CM000669.1:g.94038635G>C | GRCh37 |
NC_000007.12:g.93876571G>C | NCBI36 |
NG_007405.1:g.19763G>C , LRG_2:g.19763G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.794G>C MANE Select | ENSP00000297268.6:p.Gly265Ala | |
ENST00000297268.10:c.794G>C | ENSP00000297268.6:p.Gly265Ala | |
ENST00000620463.1:c.788G>C | ENSP00000477719.1:p.Gly263Ala | |
NM_000089.3:c.794G>C , LRG_2t1:c.794G>C | NP_000080.2:p.Gly265Ala | |
NM_000089.4:c.794G>C MANE Select | NP_000080.2:p.Gly265Ala |