HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29328392G>T , CM000664.2:g.29328392G>T | GRCh38 |
NC_000002.11:g.29551258G>T , CM000664.1:g.29551258G>T | GRCh37 |
NC_000002.10:g.29404762G>T | NCBI36 |
NG_009445.1:g.598175C>A , LRG_488:g.598175C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000389048.8:c.1372C>A MANE Select | ENSP00000373700.3:p.His458Asn | |
ENST00000389048.7:c.1372C>A | ENSP00000373700.3:p.His458Asn | |
ENST00000618119.4:c.241C>A | ENSP00000482733.1:p.His81Asn | |
NM_004304.4:c.1372C>A | NP_004295.2:p.His458Asn | |
XR_939920.1:n.700G>T | ||
XR_939921.1:n.680+5864G>T | ||
XR_001738688.2:n.2302C>A | ||
XR_939920.2:n.590G>T | ||
XR_939921.2:n.576+5864G>T | ||
NM_004304.5:c.1372C>A MANE Select | NP_004295.2:p.His458Asn |