HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38367301C>G , CM000685.2:g.38367301C>G | GRCh38 |
NC_000023.10:g.38226554C>G , CM000685.1:g.38226554C>G | GRCh37 |
NC_000023.9:g.38111498C>G | NCBI36 |
NG_008471.1:g.19819C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.88C>G MANE Select | ENSP00000039007.4:p.Pro30Ala | |
ENST00000643344.1:c.88C>G | ENSP00000496606.1:p.Pro30Ala | |
ENST00000039007.4:c.88C>G | ENSP00000039007.4:p.Pro30Ala | |
ENST00000465127.1:c.172-298820C>G | ENSP00000417050.1:n.172-298820C>G | |
ENST00000488812.1:n.180C>G | ||
NM_000531.5:c.88C>G | NP_000522.3:p.Pro30Ala | |
XM_017029556.1:c.88C>G | XP_016885045.1:p.Pro30Ala | |
NM_000531.6:c.88C>G MANE Select | NP_000522.3:p.Pro30Ala |