HGVS | Genome Assembly |
---|---|
NC_000022.11:g.39244701T>G , CM000684.2:g.39244701T>G | GRCh38 |
NC_000022.10:g.39640706T>G , CM000684.1:g.39640706T>G | GRCh37 |
NC_000022.9:g.37970652T>G | NCBI36 |
NG_012111.1:g.5252A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331163.11:c.-738A>C MANE Select | ENSP00000330382.6:n.-738A>C | |
ENST00000331163.10:c.-738A>C | ENSP00000330382.6:n.-738A>C | |
NM_002608.2:c.-738A>C | NP_002599.1:n.-738A>C | |
NM_002608.3:c.-738A>C | NP_002599.1:n.-738A>C | |
NM_002608.4:c.-738A>C MANE Select | NP_002599.1:n.-738A>C |