Canonical Allele Identifier: CA846773483
Gene: ANXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1263700097
MyVariant Identifiers: chr8:g.124714715T>G (hg19) chr8:g.123702475T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123702475T>G , CM000670.2:g.123702475T>G GRCh38
NC_000008.10:g.124714715T>G , CM000670.1:g.124714715T>G GRCh37
NC_000008.9:g.124783896T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419625.6:c.186+167A>C MANE Select ENSP00000390809.1:n.186+167A>C
ENST00000262219.10:c.309+167A>C ENSP00000262219.6:n.309+167A>C
ENST00000419625.5:c.186+167A>C ENSP00000390809.1:n.186+167A>C
ENST00000520519.1:c.99+167A>C ENSP00000429358.1:n.99+167A>C
NM_001003954.1:c.309+167A>C NP_001003954.1:n.309+167A>C
NM_004306.2:c.186+167A>C NP_004297.2:n.186+167A>C
NM_001003954.2:c.309+167A>C NP_001003954.1:n.309+167A>C
NM_004306.3:c.186+167A>C NP_004297.2:n.186+167A>C
NM_004306.4:c.186+167A>C MANE Select NP_004297.2:n.186+167A>C
NM_001003954.3:c.309+167A>C NP_001003954.1:n.309+167A>C
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