HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67753673A>G , CM000666.2:g.67753673A>G | GRCh38 |
NC_000004.11:g.68619391A>G , CM000666.1:g.68619391A>G | GRCh37 |
NC_000004.10:g.68301986A>G | NCBI36 |
NG_009293.1:g.7414T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.522+141T>C MANE Select | ENSP00000226413.5:n.522+141T>C | |
ENST00000226413.4:c.522+141T>C | ENSP00000226413.4:n.522+141T>C | |
ENST00000420975.2:c.522+141T>C | ENSP00000397561.2:n.522+141T>C | |
NM_000406.2:c.522+141T>C | NP_000397.1:n.522+141T>C | |
NM_001012763.1:c.522+141T>C | NP_001012781.1:n.522+141T>C | |
XR_938850.1:n.97A>G | ||
NM_000406.3:c.522+141T>C MANE Select | NP_000397.1:n.522+141T>C | |
NM_001012763.2:c.522+141T>C | NP_001012781.1:n.522+141T>C |