Canonical Allele Identifier: CA339300524

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761463C>G , CM000663.2:g.34761463C>G GRCh38
NC_000001.10:g.35227064C>G , CM000663.1:g.35227064C>G GRCh37
NC_000001.9:g.34999651C>G NCBI36
NG_016243.1:g.6723C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.209C>G (GJB4) MANE Select ENSP00000345868.1:p.Pro70Arg
ENST00000339480.1:c.209C>G (GJB4) ENSP00000345868.1:p.Pro70Arg
ENST00000426886.1:c.208-43054G>C (SMIM12) ENSP00000429902.1:n.208-43054G>C
NM_153212.2:c.209C>G (GJB4) NP_694944.1:p.Pro70Arg
XM_011540679.1:c.209C>G (GJB4) XP_011538981.1:p.Pro70Arg
XR_947179.1:n.1002-18014G>C
XM_011540679.2:c.209C>G (GJB4) XP_011538981.1:p.Pro70Arg
XR_001737967.1:n.1023+36908G>C
NM_153212.3:c.209C>G (GJB4) MANE Select NP_694944.1:p.Pro70Arg