HGVS | Genome Assembly |
---|---|
NC_000002.12:g.232523431C= , CM000664.2:g.232523431C= | GRCh38 |
NC_000002.11:g.233388141C= , CM000664.1:g.233388141C= | GRCh37 |
NC_000002.10:g.233096385C= | NCBI36 |
NG_008028.1:g.2220C= | |
NG_031969.1:g.7969C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000617714.2:c.865C= MANE Select | ENSP00000479745.1:p.Pro289= | |
ENST00000449534.6:c.865C= | ENSP00000473410.1:p.Pro289= | |
ENST00000617714.1:c.865C= | ENSP00000479745.1:p.Pro289= | |
NM_001195129.1:c.865C= | NP_001182058.1:p.Pro289= | |
NM_001195129.2:c.865C= MANE Select | NP_001182058.1:p.Pro289= | |
NM_001369848.1:c.865C= | NP_001356777.1:p.Pro289= |