HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15192130T= , CM000681.2:g.15192130T= | GRCh38 |
NC_000019.9:g.15302941T= , CM000681.1:g.15302941T= | GRCh37 |
NC_000019.8:g.15163941T= | NCBI36 |
NG_009819.1:g.13852A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.509A= MANE Select | ENSP00000263388.1:p.His170= | |
ENST00000263388.6:c.509A= | ENSP00000263388.1:p.His170= | |
ENST00000601011.1:c.506A= | ENSP00000473138.1:p.His169= | |
NM_000435.2:c.509A= | NP_000426.2:p.His170= | |
XM_005259924.3:c.509A= | XP_005259981.1:p.His170= | |
XM_005259924.4:c.509A= | XP_005259981.1:p.His170= | |
NM_000435.3:c.509A= MANE Select | NP_000426.2:p.His170= |