HGVS | Genome Assembly |
---|---|
NC_000014.9:g.67725110T>G , CM000676.2:g.67725110T>G | GRCh38 |
NC_000014.8:g.68191827T>G , CM000676.1:g.68191827T>G | GRCh37 |
NC_000014.7:g.67261580T>G | NCBI36 |
NG_008321.1:g.28225T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000551171.6:c.199T>G (RDH12) MANE Select | ENSP00000449079.1:p.Tyr67Asp | |
ENST00000267502.3:c.199T>G (RDH12) | ENSP00000267502.3:p.Tyr67Asp | |
ENST00000551171.5:c.199T>G (RDH12) | ENSP00000449079.1:p.Tyr67Asp | |
NM_152443.2:c.199T>G (RDH12) | NP_689656.2:p.Tyr67Asp | |
XM_017020925.2:c.1313-10085T>G (GPHN) | XP_016876414.1:n.1313-10085T>G | |
NM_152443.3:c.199T>G (RDH12) MANE Select | NP_689656.2:p.Tyr67Asp |