HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134843408T>C , CM000671.2:g.134843408T>C | GRCh38 |
NC_000009.11:g.137735254T>C , CM000671.1:g.137735254T>C | GRCh37 |
NC_000009.10:g.136875075T>C | NCBI36 |
NG_008030.1:g.206603T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.*1105T>C | ENSP00000360885.4:n.*1105T>C | |
ENST00000371817.8:c.*1105T>C MANE Select | ENSP00000360882.3:n.*1105T>C | |
ENST00000371817.7:c.*1105T>C | ENSP00000360882.3:n.*1105T>C | |
ENST00000618395.4:c.*1105T>C | ENSP00000481360.1:n.*1105T>C | |
NM_000093.4:c.*1105T>C | NP_000084.3:n.*1105T>C | |
NM_001278074.1:c.*1105T>C | NP_001265003.1:n.*1105T>C | |
NR_103451.2:n.71-23199A>G | ||
NM_000093.5:c.*1105T>C MANE Select | NP_000084.3:n.*1105T>C |