HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320357G>T , CM000667.2:g.159320357G>T | GRCh38 |
NC_000005.9:g.158747365G>T , CM000667.1:g.158747365G>T | GRCh37 |
NC_000005.8:g.158679943G>T | NCBI36 |
NG_009618.1:g.15117C>A , LRG_71:g.15117C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.16C>A | ENSP00000512849.1:p.His6Asn | |
ENST00000696751.1:c.*141C>A | ENSP00000512850.1:n.*141C>A | |
ENST00000231228.3:c.646C>A MANE Select | ENSP00000231228.2:p.His216Asn | |
ENST00000231228.2:c.646C>A | ENSP00000231228.2:p.His216Asn | |
NM_002187.2:c.646C>A , LRG_71t1:c.646C>A | NP_002178.2:p.His216Asn | |
NM_002187.3:c.646C>A MANE Select | NP_002178.2:p.His216Asn |