HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6145270A= , CM000668.2:g.6145270A= | GRCh38 |
NC_000006.11:g.6145503A= , CM000668.1:g.6145503A= | GRCh37 |
NC_000006.10:g.6090502A= | NCBI36 |
NG_008107.1:g.180422T= , LRG_549:g.180422T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.*349T= MANE Select | ENSP00000264870.3:n.*349T= | |
ENST00000264870.7:c.*349T= | ENSP00000264870.3:n.*349T= | |
NM_000129.3:c.*349T= , LRG_549t1:c.*349T= | NP_000120.2:n.*349T= | |
XM_006715010.2:c.*349T= | XP_006715073.1:n.*349T= | |
XM_011514342.1:c.*349T= | XP_011512644.1:n.*349T= | |
NM_000129.4:c.*349T= MANE Select | NP_000120.2:n.*349T= |