HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15180131C>A , CM000681.2:g.15180131C>A | GRCh38 |
NC_000019.9:g.15290942C>A , CM000681.1:g.15290942C>A | GRCh37 |
NC_000019.8:g.15151942C>A | NCBI36 |
NG_009819.1:g.25851G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263388.7:c.3268G>T MANE Select | ENSP00000263388.1:p.Ala1090Ser | |
ENST00000263388.6:c.3268G>T | ENSP00000263388.1:p.Ala1090Ser | |
ENST00000601011.1:c.3109G>T | ENSP00000473138.1:p.Ala1037Ser | |
NM_000435.2:c.3268G>T | NP_000426.2:p.Ala1090Ser | |
XM_005259924.3:c.3112G>T | XP_005259981.1:p.Ala1038Ser | |
XM_005259924.4:c.3112G>T | XP_005259981.1:p.Ala1038Ser | |
NM_000435.3:c.3268G>T MANE Select | NP_000426.2:p.Ala1090Ser |