HGVS | Genome Assembly |
---|---|
NC_000011.10:g.13492491T>A , CM000673.2:g.13492491T>A | GRCh38 |
NC_000011.9:g.13514038T>A , CM000673.1:g.13514038T>A | GRCh37 |
NC_000011.8:g.13470614T>A | NCBI36 |
NG_008962.1:g.8530A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282091.6:c.262A>T MANE Select | ENSP00000282091.1:p.Asn88Tyr | |
ENST00000282091.5:c.262A>T | ENSP00000282091.1:p.Asn88Tyr | |
ENST00000529816.1:c.262A>T | ENSP00000433208.1:p.Asn88Tyr | |
NM_000315.2:c.262A>T | NP_000306.1:p.Asn88Tyr | |
NM_000315.3:c.262A>T | NP_000306.1:p.Asn88Tyr | |
NM_001316352.1:c.358A>T | NP_001303281.1:p.Asn120Tyr | |
NM_000315.4:c.262A>T MANE Select | NP_000306.1:p.Asn88Tyr | |
NM_001316352.2:c.358A>T | NP_001303281.1:p.Asn120Tyr |