HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12790494A>G , CM000686.2:g.12790494A>G | GRCh38 |
NC_000024.9:g.14902427A>G , CM000686.1:g.14902427A>G | GRCh37 |
NC_000024.8:g.13411821A>G | NCBI36 |
NG_008311.1:g.94268A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651177.1:c.3649A>G | ENSP00000498372.1:p.Asn1217Asp | |
ENST00000338981.7:c.3649A>G MANE Select | ENSP00000342812.3:p.Asn1217Asp | |
ENST00000426564.6:n.3661A>G | ||
NM_004654.3:c.3649A>G | NP_004645.2:p.Asn1217Asp | |
XM_011531469.1:c.3649A>G | XP_011529771.1:p.Asn1217Asp | |
XM_011531470.1:c.3415A>G | XP_011529772.1:p.Asn1139Asp | |
XM_017030078.2:c.3664A>G | XP_016885567.1:p.Asn1222Asp | |
NM_004654.4:c.3649A>G MANE Select | NP_004645.2:p.Asn1217Asp |