HGVS | Genome Assembly |
---|---|
NC_000006.12:g.42721831G>A , CM000668.2:g.42721831G>A | GRCh38 |
NC_000006.11:g.42689569G>A , CM000668.1:g.42689569G>A | GRCh37 |
NC_000006.10:g.42797547G>A | NCBI36 |
NG_009176.1:g.5790C>T | |
NG_009176.2:g.5790C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230381.7:c.504C>T MANE Select | ENSP00000230381.5:p.Asn168= | |
ENST00000230381.6:c.504C>T | ENSP00000230381.5:p.Asn168= | |
NM_000322.4:c.504C>T | NP_000313.2:p.Asn168= | |
XR_427834.2:n.1159C>T | ||
XR_926295.1:n.1159C>T | ||
XR_427834.4:n.1209C>T | ||
XR_926295.3:n.1209C>T | ||
NM_000322.5:c.504C>T MANE Select | NP_000313.2:p.Asn168= |