HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42126440A>T , CM000684.2:g.42126440A>T | GRCh38 |
NC_000022.10:g.42522442A>T , CM000684.1:g.42522442A>T | GRCh37 |
NC_000022.9:g.40852386A>T | NCBI36 |
NG_008376.3:g.8552T>A | |
NG_008376.4:g.9371T>A |
HGVS | Amino-acid change | |
---|---|---|
XM_011529966.1:c.1452+176T>A | XP_011528268.1:n.1452+176T>A | |
XM_011529967.1:c.1452+176T>A | XP_011528269.1:n.1452+176T>A | |
XM_011529968.1:c.1452+176T>A | XP_011528270.1:n.1452+176T>A | |
XM_011529969.1:c.1308+176T>A | XP_011528271.1:n.1308+176T>A | |
XM_011529970.1:c.1299+176T>A | XP_011528272.1:n.1299+176T>A |