HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028940A>T , CM000667.2:g.135028940A>T | GRCh38 |
NC_000005.9:g.134364630A>T , CM000667.1:g.134364630A>T | GRCh37 |
NC_000005.8:g.134392529A>T | NCBI36 |
NG_012114.1:g.10335T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.784T>A MANE Select | ENSP00000265340.6:p.Cys262Ser | |
ENST00000265340.11:c.784T>A | ENSP00000265340.6:p.Cys262Ser | |
ENST00000506438.5:c.784T>A | ENSP00000427542.1:p.Cys262Ser | |
NM_002653.4:c.784T>A | NP_002644.4:p.Cys262Ser | |
NM_002653.5:c.784T>A MANE Select | NP_002644.4:p.Cys262Ser |