Canonical Allele Identifier: CA12852920
Gene: ANXA13 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13258681

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123702482T>C , CM000670.2:g.123702482T>C GRCh38
NC_000008.10:g.124714722T>C , CM000670.1:g.124714722T>C GRCh37
NC_000008.9:g.124783903T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001003954.1:c.309+160A>G VV NP_001003954.1:p.=
NM_004306.2:c.186+160A>G VV NP_004297.2:p.=
NM_001003954.2:c.309+160A>G VV
NM_004306.3:c.186+160A>G VV
ENST00000262219.10:c.309+160A>G ENSP00000262219.6:p.=
ENST00000419625.5:c.186+160A>G ENSP00000390809.1:p.=
ENST00000520519.1:c.99+160A>G ENSP00000429358.1:p.=