Canonical Allele Identifier: CA2706883214
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs933124664

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686018A>G , CM000666.2:g.121686018A>G GRCh38
NC_000004.11:g.122607173A>G , CM000666.1:g.122607173A>G GRCh37
NC_000004.10:g.122826623A>G NCBI36
NG_032042.1:g.15975T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+270T>C MANE Select ENSP00000296511.5:n.94+270T>C
ENST00000296511.9:c.94+270T>C ENSP00000296511.5:n.94+270T>C
ENST00000501272.6:c.10-2541T>C ENSP00000424106.1:n.10-2541T>C
ENST00000506395.5:c.94+270T>C ENSP00000421421.1:n.94+270T>C
ENST00000509016.5:n.215+270T>C
ENST00000511552.5:n.480+270T>C
ENST00000513428.5:n.259+270T>C
ENST00000513523.1:n.262+270T>C
ENST00000513728.1:c.94+270T>C ENSP00000427135.1:n.94+270T>C
ENST00000515017.5:c.94+270T>C ENSP00000424199.1:n.94+270T>C
NM_001154.3:c.94+270T>C NP_001145.1:n.94+270T>C
XM_017008141.2:c.94+270T>C XP_016863630.1:n.94+270T>C
NM_001154.4:c.94+270T>C MANE Select NP_001145.1:n.94+270T>C