HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15180427C= , CM000681.2:g.15180427C= | GRCh38 |
NC_000019.9:g.15291238C= , CM000681.1:g.15291238C= | GRCh37 |
NC_000019.8:g.15152238C= | NCBI36 |
NG_009819.1:g.25555G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.3143-171G= MANE Select | ENSP00000263388.1:n.3143-171G= | |
ENST00000263388.6:c.3143-171G= | ENSP00000263388.1:n.3143-171G= | |
ENST00000601011.1:c.2984-171G= | ENSP00000473138.1:n.2984-171G= | |
NM_000435.2:c.3143-171G= | NP_000426.2:n.3143-171G= | |
XM_005259924.3:c.2987-171G= | XP_005259981.1:n.2987-171G= | |
XM_005259924.4:c.2987-171G= | XP_005259981.1:n.2987-171G= | |
NM_000435.3:c.3143-171G= MANE Select | NP_000426.2:n.3143-171G= |