HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38075367T>A , CM000664.2:g.38075367T>A | GRCh38 |
NC_000002.11:g.38302510T>A , CM000664.1:g.38302510T>A | GRCh37 |
NC_000002.10:g.38156014T>A | NCBI36 |
NG_008386.2:g.5735A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.22A>T | ENSP00000478839.2:p.Asn8Tyr | |
ENST00000610745.5:c.22A>T MANE Select | ENSP00000478561.1:p.Asn8Tyr | |
ENST00000490576.1:c.22A>T | ENSP00000478839.1:p.Asn8Tyr | |
ENST00000494864.1:c.-70-4057A>T | ENSP00000479876.1:n.-70-4057A>T | |
ENST00000610745.4:c.22A>T | ENSP00000478561.1:p.Asn8Tyr | |
ENST00000613082.1:n.375+413A>T | ||
ENST00000614273.1:c.22A>T | ENSP00000483678.1:p.Asn8Tyr | |
NM_000104.3:c.22A>T | NP_000095.2:p.Asn8Tyr | |
NM_000104.4:c.22A>T MANE Select | NP_000095.2:p.Asn8Tyr |