HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189004094A>C , CM000664.2:g.189004094A>C | GRCh38 |
NC_000002.11:g.189868820A>C , CM000664.1:g.189868820A>C | GRCh37 |
NC_000002.10:g.189577065A>C | NCBI36 |
NG_007404.1:g.34722A>C , LRG_3:g.34722A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2675A>C | ENSP00000415346.2:p.Asp892Ala | |
ENST00000304636.9:c.2774A>C MANE Select | ENSP00000304408.4:p.Asp925Ala | |
ENST00000304636.7:c.2774A>C | ENSP00000304408.3:p.Asp925Ala | |
ENST00000317840.9:c.2527+1058A>C | ENSP00000315243.6:n.2527+1058A>C | |
NM_000090.3:c.2774A>C , LRG_3t1:c.2774A>C | NP_000081.1:p.Asp925Ala | |
NM_000090.4:c.2774A>C MANE Select | NP_000081.2:p.Asp925Ala |