HGVS | Genome Assembly |
---|---|
NC_000011.10:g.61392453T>C , CM000673.2:g.61392453T>C | GRCh38 |
NC_000011.9:g.61159925T>C , CM000673.1:g.61159925T>C | GRCh37 |
NC_000011.8:g.60916501T>C | NCBI36 |
NG_032976.1:g.5094T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000334888.9:c.-179T>C | ENSP00000334844.5:n.-179T>C | |
ENST00000398979.7:c.-376T>C | ENSP00000381950.3:n.-376T>C | |
ENST00000515837.6:c.-179T>C | ENSP00000440638.1:n.-179T>C | |
NM_001173990.2:c.-179T>C | NP_001167461.1:n.-179T>C | |
NM_001173991.2:c.-179T>C | NP_001167462.1:n.-179T>C | |
NM_016499.5:c.-376T>C | NP_057583.2:n.-376T>C | |
XM_005274039.3:c.-510T>C | XP_005274096.1:n.-510T>C | |
NM_001330285.1:c.-376T>C | NP_001317214.1:n.-376T>C | |
XM_005274039.4:c.-510T>C | XP_005274096.1:n.-510T>C |