HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121857332C>G , CM000674.2:g.121857332C>G | GRCh38 |
NC_000012.11:g.122295238C>G , CM000674.1:g.122295238C>G | GRCh37 |
NC_000012.10:g.120779621C>G | NCBI36 |
NG_016461.1:g.36280G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000289004.8:c.194G>C (HPD) MANE Select | ENSP00000289004.4:p.Gly65Ala | |
ENST00000535114.1:n.550G>C (HPD) | ||
ENST00000542159.2:n.252G>C (HPD) | ||
ENST00000543163.5:c.77G>C (HPD) | ENSP00000441677.1:p.Gly26Ala | |
NM_001171993.1:c.77G>C (HPD) | NP_001165464.1:p.Gly26Ala | |
NM_002150.2:c.194G>C (HPD) | NP_002141.1:p.Gly65Ala | |
XR_002957437.1:n.324-287C>G (TIALD) | ||
NM_002150.3:c.194G>C (HPD) MANE Select | NP_002141.2:p.Gly65Ala | |
NM_001171993.2:c.77G>C (HPD) | NP_001165464.1:p.Gly26Ala |