HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125388C>G , CM000666.2:g.55125388C>G | GRCh38 |
NC_000004.11:g.55991555C>G , CM000666.1:g.55991555C>G | GRCh37 |
NC_000004.10:g.55686312C>G | NCBI36 |
NG_012004.1:g.5208G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-95G>C MANE Select | ENSP00000263923.4:n.-95G>C | |
ENST00000263923.4:c.-95G>C | ENSP00000263923.4:n.-95G>C | |
NM_002253.2:c.-95G>C | NP_002244.1:n.-95G>C | |
NM_002253.3:c.-95G>C | NP_002244.1:n.-95G>C | |
NM_002253.4:c.-95G>C MANE Select | NP_002244.1:n.-95G>C |