HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160424988G>T , CM000663.2:g.160424988G>T | GRCh38 |
NC_000001.10:g.160394778G>T , CM000663.1:g.160394778G>T | GRCh37 |
NC_000001.9:g.158661402G>T | NCBI36 |
NG_023420.1:g.29415G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696602.1:c.1450-130G>T | ENSP00000512747.1:n.1450-130G>T | |
ENST00000368061.3:c.1306-130G>T MANE Select | ENSP00000357040.2:n.1306-130G>T | |
ENST00000368061.2:c.1306-130G>T | ENSP00000357040.2:n.1306-130G>T | |
NM_020335.2:c.1306-130G>T | NP_065068.1:n.1306-130G>T | |
XM_005245357.1:c.1306-130G>T | XP_005245414.1:n.1306-130G>T | |
XM_011509804.1:c.1306-130G>T | XP_011508106.1:n.1306-130G>T | |
NM_020335.3:c.1306-130G>T MANE Select | NP_065068.1:n.1306-130G>T |