HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14125098T>C , CM000665.2:g.14125098T>C | GRCh38 |
NC_000003.11:g.14166598T>C , CM000665.1:g.14166598T>C | GRCh37 |
NC_000003.10:g.14141599T>C | NCBI36 |
NG_008975.1:g.5159T>C , LRG_435:g.5159T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432444.2:c.-96T>C | ENSP00000395617.1:n.-96T>C | |
ENST00000306077.5:c.-96T>C MANE Select | ENSP00000303992.5:n.-96T>C | |
ENST00000306077.4:c.-96T>C | ENSP00000303992.4:n.-96T>C | |
ENST00000432444.1:c.-96T>C | ENSP00000395617.1:n.-96T>C | |
NM_024334.2:c.-96T>C , LRG_435t1:c.-96T>C | NP_077310.1:n.-96T>C | |
XM_017007176.2:c.-432T>C | XP_016862665.1:n.-432T>C | |
NM_024334.3:c.-96T>C MANE Select | NP_077310.1:n.-96T>C |