Canonical Allele Identifier: CA417248394

Linked Data

MyVariant Identifiers: chr1:g.35227056G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34761455G>A , CM000663.2:g.34761455G>A GRCh38
NC_000001.10:g.35227056G>A , CM000663.1:g.35227056G>A GRCh37
NC_000001.9:g.34999643G>A NCBI36
NG_016243.1:g.6715G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339480.3:c.201G>A (GJB4) MANE Select ENSP00000345868.1:p.Glu67=
ENST00000339480.1:c.201G>A (GJB4) ENSP00000345868.1:p.Glu67=
ENST00000426886.1:c.208-43046C>T (SMIM12) ENSP00000429902.1:n.208-43046C>T
NM_153212.2:c.201G>A (GJB4) NP_694944.1:p.Glu67=
XM_011540679.1:c.201G>A (GJB4) XP_011538981.1:p.Glu67=
XR_947179.1:n.1002-18006C>T
XM_011540679.2:c.201G>A (GJB4) XP_011538981.1:p.Glu67=
XR_001737967.1:n.1023+36916C>T
NM_153212.3:c.201G>A (GJB4) MANE Select NP_694944.1:p.Glu67=