HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43928907G>T , CM000684.2:g.43928907G>T | GRCh38 |
NC_000022.10:g.44324787G>T , CM000684.1:g.44324787G>T | GRCh37 |
NC_000022.9:g.42656120G>T | NCBI36 |
NG_008631.1:g.10169G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216180.8:c.486+18G>T MANE Select | ENSP00000216180.3:n.486+18G>T | |
ENST00000216180.7:c.486+18G>T | ENSP00000216180.3:n.486+18G>T | |
ENST00000406117.6:c.*118+18G>T | ENSP00000384668.2:n.*118+18G>T | |
ENST00000423180.2:c.474+18G>T | ENSP00000397987.2:n.474+18G>T | |
ENST00000478713.1:n.520+18G>T | ||
NM_025225.2:c.486+18G>T | NP_079501.2:n.486+18G>T | |
NM_025225.3:c.486+18G>T MANE Select | NP_079501.2:n.486+18G>T |