HGVS | Genome Assembly |
---|---|
NC_000011.10:g.61392474G>T , CM000673.2:g.61392474G>T | GRCh38 |
NC_000011.9:g.61159946G>T , CM000673.1:g.61159946G>T | GRCh37 |
NC_000011.8:g.60916522G>T | NCBI36 |
NG_032976.1:g.5115G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000334888.9:c.-158G>T | ENSP00000334844.5:n.-158G>T | |
ENST00000398979.7:c.-355G>T | ENSP00000381950.3:n.-355G>T | |
ENST00000515837.6:c.-158G>T | ENSP00000440638.1:n.-158G>T | |
NM_001173990.2:c.-158G>T | NP_001167461.1:n.-158G>T | |
NM_001173991.2:c.-158G>T | NP_001167462.1:n.-158G>T | |
NM_016499.5:c.-355G>T | NP_057583.2:n.-355G>T | |
XM_005274039.3:c.-489G>T | XP_005274096.1:n.-489G>T | |
NM_001330285.1:c.-355G>T | NP_001317214.1:n.-355G>T | |
XM_005274039.4:c.-489G>T | XP_005274096.1:n.-489G>T |