HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15191694G= , CM000681.2:g.15191694G= | GRCh38 |
NC_000019.9:g.15302505G= , CM000681.1:g.15302505G= | GRCh37 |
NC_000019.8:g.15163505G= | NCBI36 |
NG_009819.1:g.14288C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.803-37C= MANE Select | ENSP00000263388.1:n.803-37C= | |
ENST00000263388.6:c.803-37C= | ENSP00000263388.1:n.803-37C= | |
ENST00000601011.1:c.800-37C= | ENSP00000473138.1:n.800-37C= | |
NM_000435.2:c.803-37C= | NP_000426.2:n.803-37C= | |
XM_005259924.3:c.803-37C= | XP_005259981.1:n.803-37C= | |
XM_005259924.4:c.803-37C= | XP_005259981.1:n.803-37C= | |
NM_000435.3:c.803-37C= MANE Select | NP_000426.2:n.803-37C= |