HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38074943T>G , CM000664.2:g.38074943T>G | GRCh38 |
NC_000002.11:g.38302086T>G , CM000664.1:g.38302086T>G | GRCh37 |
NC_000002.10:g.38155590T>G | NCBI36 |
NG_008386.2:g.6159A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000490576.2:c.446A>C | ENSP00000478839.2:p.His149Pro | |
ENST00000610745.5:c.446A>C MANE Select | ENSP00000478561.1:p.His149Pro | |
ENST00000494864.1:c.-70-3633A>C | ENSP00000479876.1:n.-70-3633A>C | |
ENST00000610745.4:c.446A>C | ENSP00000478561.1:p.His149Pro | |
ENST00000613082.1:n.376-535A>C | ||
ENST00000614273.1:c.446A>C | ENSP00000483678.1:p.His149Pro | |
NM_000104.3:c.446A>C | NP_000095.2:p.His149Pro | |
NM_000104.4:c.446A>C MANE Select | NP_000095.2:p.His149Pro |