Canonical Allele Identifier: CA339300641

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761477C>G , CM000663.2:g.34761477C>G GRCh38
NC_000001.10:g.35227078C>G , CM000663.1:g.35227078C>G GRCh37
NC_000001.9:g.34999665C>G NCBI36
NG_016243.1:g.6737C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.223C>G (GJB4) MANE Select ENSP00000345868.1:p.Arg75Gly
ENST00000339480.1:c.223C>G (GJB4) ENSP00000345868.1:p.Arg75Gly
ENST00000426886.1:c.208-43068G>C (SMIM12) ENSP00000429902.1:n.208-43068G>C
NM_153212.2:c.223C>G (GJB4) NP_694944.1:p.Arg75Gly
XM_011540679.1:c.223C>G (GJB4) XP_011538981.1:p.Arg75Gly
XR_947179.1:n.1002-18028G>C
XM_011540679.2:c.223C>G (GJB4) XP_011538981.1:p.Arg75Gly
XR_001737967.1:n.1023+36894G>C
NM_153212.3:c.223C>G (GJB4) MANE Select NP_694944.1:p.Arg75Gly