HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7526763C= , CM000681.2:g.7526763C= | GRCh38 |
NC_000019.9:g.7591649C= , CM000681.1:g.7591649C= | GRCh37 |
NC_000019.8:g.7497649C= | NCBI36 |
NG_015806.1:g.9154C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.408C= MANE Select | ENSP00000264079.5:p.Tyr136= | |
ENST00000264079.10:c.408C= | ENSP00000264079.5:p.Tyr136= | |
ENST00000394321.9:n.488C= | ||
ENST00000596008.1:n.370C= | ||
ENST00000598406.1:n.229C= | ||
ENST00000601003.1:c.408C= | ENSP00000469074.1:p.Tyr136= | |
NM_020533.2:c.408C= | NP_065394.1:p.Tyr136= | |
NM_020533.3:c.408C= MANE Select | NP_065394.1:p.Tyr136= |