Canonical Allele Identifier: CA417249107

Linked Data

dbSNP Id: rs2148357913
MyVariant Identifiers: chr1:g.35259967T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794366T>C , CM000663.2:g.34794366T>C GRCh38
NC_000001.10:g.35259967T>C , CM000663.1:g.35259967T>C GRCh37
NC_000001.9:g.35032554T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000342280.5:c.153T>C (GJA4) MANE Select ENSP00000343676.4:p.Asp51=
ENST00000342280.4:c.153T>C (GJA4) ENSP00000343676.4:p.Asp51=
ENST00000426886.1:c.207+61405A>G (SMIM12) ENSP00000429902.1:n.207+61405A>G
ENST00000450137.1:c.153T>C (GJA4) ENSP00000409186.1:p.Asp51=
NM_002060.2:c.153T>C (GJA4) NP_002051.2:p.Asp51=
XM_005270750.1:c.153T>C (GJA4) XP_005270807.1:p.Asp51=
XR_947179.1:n.1001+4005A>G
XM_005270750.2:c.153T>C (GJA4) XP_005270807.1:p.Asp51=
XM_017001043.2:c.153T>C (GJA4) XP_016856532.1:p.Asp51=
XR_001737967.1:n.1023+4005A>G
NM_002060.3:c.153T>C (GJA4) MANE Select NP_002051.2:p.Asp51=