HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951831A>G , CM000670.2:g.19951831A>G | GRCh38 |
NC_000008.10:g.19809342A>G , CM000670.1:g.19809342A>G | GRCh37 |
NC_000008.9:g.19853622A>G | NCBI36 |
NG_008855.1:g.17761A>G | |
NG_008855.2:g.55115A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.312A>G MANE Select | ENSP00000497642.1:p.Pro104= | |
ENST00000311322.8:c.312A>G | ENSP00000309757.6:p.Pro104= | |
ENST00000520959.5:c.84A>G | ENSP00000428496.1:p.Pro28= | |
ENST00000522701.5:c.312A>G | ENSP00000428557.1:p.Pro104= | |
ENST00000524029.5:c.312A>G | ENSP00000428237.1:p.Pro104= | |
NM_000237.2:c.312A>G | NP_000228.1:p.Pro104= | |
NM_000237.3:c.312A>G MANE Select | NP_000228.1:p.Pro104= |