HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48381412A= , CM000675.2:g.48381412A= | GRCh38 |
NC_000013.10:g.48955548A= , CM000675.1:g.48955548A= | GRCh37 |
NC_000013.9:g.47853549A= | NCBI36 |
NG_009009.1:g.82666A= , LRG_517:g.82666A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000267163.6:c.1664A= MANE Select | ENSP00000267163.4:p.His555= | |
ENST00000643064.1:c.163A= | ||
ENST00000650461.1:c.1664A= | ENSP00000497193.1:p.His555= | |
ENST00000267163.4:c.1664A= | ENSP00000267163.4:p.His555= | |
NM_000321.2:c.1664A= , LRG_517t1:c.1664A= | NP_000312.2:p.His555= | |
XM_011535171.1:c.1403A= | XP_011533473.1:p.His468= | |
XM_011535171.2:c.1403A= | XP_011533473.1:p.His468= | |
NM_000321.3:c.1664A= MANE Select | NP_000312.2:p.His555= |