HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155140056G>A , CM000663.2:g.155140056G>A | GRCh38 |
NC_000001.10:g.155112532G>A , CM000663.1:g.155112532G>A | GRCh37 |
NC_000001.9:g.153379156G>A | NCBI36 |
NG_012871.1:g.5465C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368400.5:c.185C>T MANE Select | ENSP00000357385.5:p.Ala62Val | |
ENST00000341298.3:c.185C>T | ENSP00000344338.3:p.Ala62Val | |
ENST00000368399.1:c.275C>T | ENSP00000357384.1:p.Ala92Val | |
ENST00000368400.4:c.185C>T | ENSP00000357385.4:p.Ala62Val | |
NM_018973.3:c.275C>T | NP_061846.2:p.Ala92Val | |
NM_153741.1:c.185C>T | NP_714963.1:p.Ala62Val | |
XM_017001498.1:c.185C>T | XP_016856987.1:p.Ala62Val | |
NM_153741.2:c.185C>T MANE Select | NP_714963.1:p.Ala62Val | |
NM_018973.4:c.275C>T | NP_061846.2:p.Ala92Val |