HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121857389G>A , CM000674.2:g.121857389G>A | GRCh38 |
NC_000012.11:g.122295295G>A , CM000674.1:g.122295295G>A | GRCh37 |
NC_000012.10:g.120779678G>A | NCBI36 |
NG_016461.1:g.36223C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289004.8:c.137C>T (HPD) MANE Select | ENSP00000289004.4:p.Ala46Val | |
ENST00000535114.1:n.493C>T (HPD) | ||
ENST00000542159.2:n.195C>T (HPD) | ||
ENST00000543163.5:c.20C>T (HPD) | ENSP00000441677.1:p.Ala7Val | |
NM_001171993.1:c.20C>T (HPD) | NP_001165464.1:p.Ala7Val | |
NM_002150.2:c.137C>T (HPD) | NP_002141.1:p.Ala46Val | |
XR_002957437.1:n.324-230G>A (TIALD) | ||
NM_002150.3:c.137C>T (HPD) MANE Select | NP_002141.2:p.Ala46Val | |
NM_001171993.2:c.20C>T (HPD) | NP_001165464.1:p.Ala7Val |