Canonical Allele Identifier: CA339300802

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761496T>G , CM000663.2:g.34761496T>G GRCh38
NC_000001.10:g.35227097T>G , CM000663.1:g.35227097T>G GRCh37
NC_000001.9:g.34999684T>G NCBI36
NG_016243.1:g.6756T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.242T>G (GJB4) MANE Select ENSP00000345868.1:p.Leu81Arg
ENST00000339480.1:c.242T>G (GJB4) ENSP00000345868.1:p.Leu81Arg
ENST00000426886.1:c.208-43087A>C (SMIM12) ENSP00000429902.1:n.208-43087A>C
NM_153212.2:c.242T>G (GJB4) NP_694944.1:p.Leu81Arg
XM_011540679.1:c.242T>G (GJB4) XP_011538981.1:p.Leu81Arg
XR_947179.1:n.1002-18047A>C
XM_011540679.2:c.242T>G (GJB4) XP_011538981.1:p.Leu81Arg
XR_001737967.1:n.1023+36875A>C
NM_153212.3:c.242T>G (GJB4) MANE Select NP_694944.1:p.Leu81Arg