Canonical Allele Identifier: CA1118741969

Gene: ANXA13

Linked Data

• dbSNP Id: rs1813461509
• gnomAD v3: 8-123702452-G-C
• gnomAD v4: 8-123702452-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702452G>C , CM000670.2:g.123702452G>C	GRCh38
NC_000008.10:g.124714692G>C , CM000670.1:g.124714692G>C	GRCh37
NC_000008.9:g.124783873G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419625.6:c.186+190C>G MANE Select	ENSP00000390809.1:n.186+190C>G
ENST00000262219.10:c.309+190C>G	ENSP00000262219.6:n.309+190C>G
ENST00000419625.5:c.186+190C>G	ENSP00000390809.1:n.186+190C>G
ENST00000520519.1:c.99+190C>G	ENSP00000429358.1:n.99+190C>G
NM_001003954.1:c.309+190C>G	NP_001003954.1:n.309+190C>G
NM_004306.2:c.186+190C>G	NP_004297.2:n.186+190C>G
NM_001003954.2:c.309+190C>G	NP_001003954.1:n.309+190C>G
NM_004306.3:c.186+190C>G	NP_004297.2:n.186+190C>G
NM_004306.4:c.186+190C>G MANE Select	NP_004297.2:n.186+190C>G
NM_001003954.3:c.309+190C>G	NP_001003954.1:n.309+190C>G