HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884776T>A , CM000680.2:g.13884776T>A | GRCh38 |
NC_000018.9:g.13884775T>A , CM000680.1:g.13884775T>A | GRCh37 |
NC_000018.8:g.13874775T>A | NCBI36 |
NG_011819.1:g.35761A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327606.4:c.743A>T MANE Select | ENSP00000333821.2:p.Asn248Ile | |
ENST00000327606.3:c.743A>T | ENSP00000333821.2:p.Asn248Ile | |
NM_000529.2:c.743A>T MANE Select | NP_000520.1:p.Asn248Ile | |
NM_001291911.1:c.743A>T | NP_001278840.1:p.Asn248Ile | |
XM_017025781.1:c.743A>T | XP_016881270.1:p.Asn248Ile |