HGVS | Genome Assembly |
---|---|
NC_000011.10:g.17642138C>T , CM000673.2:g.17642138C>T | GRCh38 |
NC_000011.9:g.17663685C>T , CM000673.1:g.17663685C>T | GRCh37 |
NC_000011.8:g.17620261C>T | NCBI36 |
NG_033191.1:g.99766C>T | |
NG_033191.2:g.99766C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399391.7:c.8343C>T | ENSP00000382323.2:p.Ser2781= | |
ENST00000399397.6:c.8307C>T MANE Select | ENSP00000382329.2:p.Ser2769= | |
ENST00000399391.6:c.8343C>T | ENSP00000382323.2:p.Ser2781= | |
ENST00000399397.5:c.8307C>T | ENSP00000382329.2:p.Ser2769= | |
NM_001277269.1:c.8343C>T | NP_001264198.1:p.Ser2781= | |
NM_001292063.1:c.8307C>T | NP_001278992.1:p.Ser2769= | |
NM_001277269.2:c.8343C>T | NP_001264198.1:p.Ser2781= | |
NM_001292063.2:c.8307C>T MANE Select | NP_001278992.1:p.Ser2769= |