HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21816640A>T , CM000669.2:g.21816640A>T | GRCh38 |
NC_000007.13:g.21856258A>T , CM000669.1:g.21856258A>T | GRCh37 |
NC_000007.12:g.21822783A>T | NCBI36 |
NG_012886.2:g.278426A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.10506A>T MANE Select | ENSP00000475939.1:p.Gly3502= | |
ENST00000328843.10:c.10527A>T | ENSP00000330671.7:p.Gly3509= | |
ENST00000409508.7:c.10506A>T | ENSP00000475939.1:p.Gly3502= | |
ENST00000620169.4:c.10527A>T | ENSP00000481693.1:p.Gly3509= | |
NM_001277115.1:c.10506A>T | NP_001264044.1:p.Gly3502= | |
NM_001277115.2:c.10506A>T MANE Select | NP_001264044.1:p.Gly3502= |