HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816309C>G , CM000681.2:g.4816309C>G | GRCh38 |
NC_000019.9:g.4816321C>G , CM000681.1:g.4816321C>G | GRCh37 |
NC_000019.8:g.4767321C>G | NCBI36 |
NG_031998.1:g.20434G>C , LRG_358:g.20434G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.2069G>C MANE Select | ENSP00000248244.4:p.Gly690Ala | |
ENST00000248244.5:c.2069G>C | ENSP00000248244.4:p.Gly690Ala | |
ENST00000621756.1:c.1571G>C | ENSP00000479467.1:p.Gly524Ala | |
NM_182919.3:c.2069G>C , LRG_358t1:c.2069G>C | NP_891549.1:p.Gly690Ala | |
NM_001385678.1:c.2027G>C | NP_001372607.1:p.Gly676Ala | |
NM_001385679.1:c.1934G>C | NP_001372608.1:p.Gly645Ala | |
NM_001385680.1:c.1427G>C | NP_001372609.1:p.Gly476Ala | |
NM_182919.4:c.2069G>C MANE Select | NP_891549.1:p.Gly690Ala |