HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190310220C>A , CM000665.2:g.190310220C>A | GRCh38 |
NC_000003.11:g.190028009C>A , CM000665.1:g.190028009C>A | GRCh37 |
NC_000003.10:g.191510703C>A | NCBI36 |
NG_021418.1:g.17227G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295522.4:c.422G>T (CLDN1) MANE Select | ENSP00000295522.3:p.Gly141Val | |
ENST00000295522.3:c.422G>T (CLDN1) | ENSP00000295522.3:p.Gly141Val | |
ENST00000490800.1:n.381G>T (CLDN1) | ||
NM_021101.4:c.422G>T (CLDN1) | NP_066924.1:p.Gly141Val | |
XR_001741069.1:n.203-4673C>A | ||
NM_021101.5:c.422G>T (CLDN1) MANE Select | NP_066924.1:p.Gly141Val | |
NM_001378492.1:c.-445-4673C>A (CLDN16) | NP_001365421.1:n.-445-4673C>A | |
NM_001378493.1:c.-279+19629C>A (CLDN16) | NP_001365422.1:n.-279+19629C>A |