Canonical Allele Identifier: CA339300603

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761472A>C , CM000663.2:g.34761472A>C GRCh38
NC_000001.10:g.35227073A>C , CM000663.1:g.35227073A>C GRCh37
NC_000001.9:g.34999660A>C NCBI36
NG_016243.1:g.6732A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.218A>C (GJB4) MANE Select ENSP00000345868.1:p.His73Pro
ENST00000339480.1:c.218A>C (GJB4) ENSP00000345868.1:p.His73Pro
ENST00000426886.1:c.208-43063T>G (SMIM12) ENSP00000429902.1:n.208-43063T>G
NM_153212.2:c.218A>C (GJB4) NP_694944.1:p.His73Pro
XM_011540679.1:c.218A>C (GJB4) XP_011538981.1:p.His73Pro
XR_947179.1:n.1002-18023T>G
XM_011540679.2:c.218A>C (GJB4) XP_011538981.1:p.His73Pro
XR_001737967.1:n.1023+36899T>G
NM_153212.3:c.218A>C (GJB4) MANE Select NP_694944.1:p.His73Pro