Canonical Allele Identifier: CA11910103
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs6830321

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693600C>T , CM000666.2:g.121693600C>T GRCh38
NC_000004.11:g.122614755C>T , CM000666.1:g.122614755C>T GRCh37
NC_000004.10:g.122834205C>T NCBI36
NG_032042.1:g.8393G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+2981G>A MANE Select ENSP00000296511.5:p.=
ENST00000296511.9:c.9+2981G>A ENSP00000296511.5:p.=
ENST00000501272.6:c.9+2981G>A ENSP00000424106.1:p.=
ENST00000506395.5:c.9+2981G>A ENSP00000421421.1:p.=
ENST00000509016.5:n.130+3263G>A
ENST00000511552.5:n.395+2981G>A
ENST00000513428.5:n.174+2981G>A
ENST00000513523.1:n.177+2981G>A
ENST00000513728.1:c.9+2981G>A ENSP00000427135.1:p.=
ENST00000515017.5:c.9+2981G>A ENSP00000424199.1:p.=
NM_001154.3:c.9+2981G>A NP_001145.1:p.=
XM_017008141.2:c.9+2981G>A XP_016863630.1:p.=
NM_001154.4:c.9+2981G>A MANE Select NP_001145.1:p.=