Canonical Allele Identifier: CA846773565

Gene: ANXA13

Linked Data

• dbSNP Id: rs1295836133
• gnomAD v3: 8-123702604-T-C
• gnomAD v4: 8-123702604-T-C
• MyVariant Identifiers: chr8:g.124714844T>C (hg19) ; chr8:g.123702604T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702604T>C , CM000670.2:g.123702604T>C	GRCh38
NC_000008.10:g.124714844T>C , CM000670.1:g.124714844T>C	GRCh37
NC_000008.9:g.124784025T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419625.6:c.186+38A>G MANE Select	ENSP00000390809.1:n.186+38A>G
ENST00000262219.10:c.309+38A>G	ENSP00000262219.6:n.309+38A>G
ENST00000419625.5:c.186+38A>G	ENSP00000390809.1:n.186+38A>G
ENST00000520519.1:c.99+38A>G	ENSP00000429358.1:n.99+38A>G
NM_001003954.1:c.309+38A>G	NP_001003954.1:n.309+38A>G
NM_004306.2:c.186+38A>G	NP_004297.2:n.186+38A>G
NM_001003954.2:c.309+38A>G	NP_001003954.1:n.309+38A>G
NM_004306.3:c.186+38A>G	NP_004297.2:n.186+38A>G
NM_004306.4:c.186+38A>G MANE Select	NP_004297.2:n.186+38A>G
NM_001003954.3:c.309+38A>G	NP_001003954.1:n.309+38A>G