Canonical Allele Identifier: CA754503

Linked Data

dbSNP Id: rs76188300
gnomAD v2: 1-35227041-C-G
gnomAD v4: 1-34761440-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761440C>G , CM000663.2:g.34761440C>G GRCh38
NC_000001.10:g.35227041C>G , CM000663.1:g.35227041C>G GRCh37
NC_000001.9:g.34999628C>G NCBI36
NG_016243.1:g.6700C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.186C>G (GJB4) MANE Select ENSP00000345868.1:p.Asn62Lys
ENST00000339480.1:c.186C>G (GJB4) ENSP00000345868.1:p.Asn62Lys
ENST00000426886.1:c.208-43031G>C (SMIM12) ENSP00000429902.1:n.208-43031G>C
NM_153212.2:c.186C>G (GJB4) NP_694944.1:p.Asn62Lys
XM_011540679.1:c.186C>G (GJB4) XP_011538981.1:p.Asn62Lys
XR_947179.1:n.1002-17991G>C
XM_011540679.2:c.186C>G (GJB4) XP_011538981.1:p.Asn62Lys
XR_001737967.1:n.1023+36931G>C
NM_153212.3:c.186C>G (GJB4) MANE Select NP_694944.1:p.Asn62Lys