Canonical Allele Identifier: CA2706981023
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs2110487587

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685918T>C , CM000666.2:g.121685918T>C GRCh38
NC_000004.11:g.122607073T>C , CM000666.1:g.122607073T>C GRCh37
NC_000004.10:g.122826523T>C NCBI36
NG_032042.1:g.16075A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+370A>G MANE Select ENSP00000296511.5:n.94+370A>G
ENST00000296511.9:c.94+370A>G ENSP00000296511.5:n.94+370A>G
ENST00000501272.6:c.10-2441A>G ENSP00000424106.1:n.10-2441A>G
ENST00000506395.5:c.94+370A>G ENSP00000421421.1:n.94+370A>G
ENST00000509016.5:n.215+370A>G
ENST00000511552.5:n.480+370A>G
ENST00000513428.5:n.259+370A>G
ENST00000513523.1:n.262+370A>G
ENST00000513728.1:c.94+370A>G ENSP00000427135.1:n.94+370A>G
ENST00000515017.5:c.94+370A>G ENSP00000424199.1:n.94+370A>G
NM_001154.3:c.94+370A>G NP_001145.1:n.94+370A>G
XM_017008141.2:c.94+370A>G XP_016863630.1:n.94+370A>G
NM_001154.4:c.94+370A>G MANE Select NP_001145.1:n.94+370A>G