HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43183043T>C , CM000684.2:g.43183043T>C | GRCh38 |
NC_000022.10:g.43579049T>C , CM000684.1:g.43579049T>C | GRCh37 |
NC_000022.9:g.41908993T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216129.7:c.284A>G MANE Select | ENSP00000216129.6:p.Asn95Ser | |
ENST00000216129.6:c.284A>G | ENSP00000216129.6:p.Asn95Ser | |
NM_015140.3:c.284A>G | NP_055955.1:p.Asn95Ser | |
XM_011530015.1:c.77A>G | XP_011528317.1:p.Asn26Ser | |
NM_015140.4:c.284A>G MANE Select | NP_055955.1:p.Asn95Ser |