HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190322102A>G , CM000665.2:g.190322102A>G | GRCh38 |
NC_000003.11:g.190039891A>G , CM000665.1:g.190039891A>G | GRCh37 |
NC_000003.10:g.191522585A>G | NCBI36 |
NG_021418.1:g.5345T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295522.4:c.105T>C (CLDN1) MANE Select | ENSP00000295522.3:p.Tyr35= | |
ENST00000295522.3:c.105T>C (CLDN1) | ENSP00000295522.3:p.Tyr35= | |
NM_021101.4:c.105T>C (CLDN1) | NP_066924.1:p.Tyr35= | |
NM_021101.5:c.105T>C (CLDN1) MANE Select | NP_066924.1:p.Tyr35= | |
NM_001378492.1:c.-279+7043A>G (CLDN16) | NP_001365421.1:n.-279+7043A>G | |
NM_001378493.1:c.-279+31511A>G (CLDN16) | NP_001365422.1:n.-279+31511A>G |