HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44251252C>T , CM000679.2:g.44251252C>T | GRCh38 |
NC_000017.10:g.42328620C>T , CM000679.1:g.42328620C>T | GRCh37 |
NC_000017.9:g.39684146C>T | NCBI36 |
NG_007498.1:g.21883G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262418.12:c.2562G>A MANE Select | ENSP00000262418.6:p.Pro854= | |
ENST00000262418.10:c.2562G>A | ENSP00000262418.6:p.Pro854= | |
ENST00000399246.3:c.1464G>A | ENSP00000382190.3:p.Pro488= | |
NM_000342.3:c.2562G>A | NP_000333.1:p.Pro854= | |
XM_005257593.3:c.2367G>A | XP_005257650.1:p.Pro789= | |
XM_011525129.1:c.2472G>A | XP_011523431.1:p.Pro824= | |
XM_005257593.5:c.2367G>A | XP_005257650.1:p.Pro789= | |
XM_011525129.2:c.2472G>A | XP_011523431.1:p.Pro824= | |
NM_000342.4:c.2562G>A MANE Select | NP_000333.1:p.Pro854= |