HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190310231T>C , CM000665.2:g.190310231T>C | GRCh38 |
NC_000003.11:g.190028020T>C , CM000665.1:g.190028020T>C | GRCh37 |
NC_000003.10:g.191510714T>C | NCBI36 |
NG_021418.1:g.17216A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295522.4:c.411A>G (CLDN1) MANE Select | ENSP00000295522.3:p.Thr137= | |
ENST00000295522.3:c.411A>G (CLDN1) | ENSP00000295522.3:p.Thr137= | |
ENST00000490800.1:n.370A>G (CLDN1) | ||
NM_021101.4:c.411A>G (CLDN1) | NP_066924.1:p.Thr137= | |
XR_001741069.1:n.203-4662T>C | ||
NM_021101.5:c.411A>G (CLDN1) MANE Select | NP_066924.1:p.Thr137= | |
NM_001378492.1:c.-445-4662T>C (CLDN16) | NP_001365421.1:n.-445-4662T>C | |
NM_001378493.1:c.-279+19640T>C (CLDN16) | NP_001365422.1:n.-279+19640T>C |