HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659625T>C , CM000683.2:g.31659625T>C | GRCh38 |
NC_000021.8:g.33031938T>C , CM000683.1:g.33031938T>C | GRCh37 |
NC_000021.7:g.31953809T>C | NCBI36 |
NG_008689.1:g.5004T>C , LRG_652:g.5004T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.10:c.-145T>C | ENSP00000270142.6:n.-145T>C | |
NM_000454.4:c.-145T>C , LRG_652t1:c.-145T>C | NP_000445.1:n.-145T>C |