HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190322158C= , CM000665.2:g.190322158C= | GRCh38 |
NC_000003.11:g.190039947C= , CM000665.1:g.190039947C= | GRCh37 |
NC_000003.10:g.191522641C= | NCBI36 |
NG_021418.1:g.5289G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295522.4:c.49G= (CLDN1) MANE Select | ENSP00000295522.3:p.Gly17= | |
ENST00000295522.3:c.49G= (CLDN1) | ENSP00000295522.3:p.Gly17= | |
NM_021101.4:c.49G= (CLDN1) | NP_066924.1:p.Gly17= | |
NM_021101.5:c.49G= (CLDN1) MANE Select | NP_066924.1:p.Gly17= | |
NM_001378492.1:c.-279+7099C= (CLDN16) | NP_001365421.1:n.-279+7099C= | |
NM_001378493.1:c.-279+31567C= (CLDN16) | NP_001365422.1:n.-279+31567C= |