HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119413506T= , CM000665.2:g.119413506T= | GRCh38 |
NC_000003.11:g.119132353T= , CM000665.1:g.119132353T= | GRCh37 |
NC_000003.10:g.120615043T= | NCBI36 |
NG_007665.2:g.124134T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.1927-350T= MANE Select | ENSP00000264245.4:n.1927-350T= | |
ENST00000264245.8:c.1927-350T= | ENSP00000264245.4:n.1927-350T= | |
NM_020754.3:c.1927-350T= | NP_065805.2:n.1927-350T= | |
XM_005247671.3:c.1834-350T= | XP_005247728.1:n.1834-350T= | |
XM_006713714.2:c.1867-350T= | XP_006713777.1:n.1867-350T= | |
XM_006713714.3:c.1867-350T= | XP_006713777.1:n.1867-350T= | |
XM_017006955.1:c.1435-350T= | XP_016862444.1:n.1435-350T= | |
NM_020754.4:c.1927-350T= MANE Select | NP_065805.2:n.1927-350T= |