HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190322173T>A , CM000665.2:g.190322173T>A | GRCh38 |
NC_000003.11:g.190039962T>A , CM000665.1:g.190039962T>A | GRCh37 |
NC_000003.10:g.191522656T>A | NCBI36 |
NG_021418.1:g.5274A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295522.4:c.34A>T (CLDN1) MANE Select | ENSP00000295522.3:p.Ile12Phe | |
ENST00000295522.3:c.34A>T (CLDN1) | ENSP00000295522.3:p.Ile12Phe | |
NM_021101.4:c.34A>T (CLDN1) | NP_066924.1:p.Ile12Phe | |
NM_021101.5:c.34A>T (CLDN1) MANE Select | NP_066924.1:p.Ile12Phe | |
NM_001378492.1:c.-279+7114T>A (CLDN16) | NP_001365421.1:n.-279+7114T>A | |
NM_001378493.1:c.-279+31582T>A (CLDN16) | NP_001365422.1:n.-279+31582T>A |