Canonical Allele Identifier: CA1489956985
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1725098759
gnomAD v4: 4-121696992-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696992C>T , CM000666.2:g.121696992C>T GRCh38
NC_000004.11:g.122618147C>T , CM000666.1:g.122618147C>T GRCh37
NC_000004.10:g.122837597C>T NCBI36
NG_032042.1:g.5001G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-165G>A ENSP00000296511.5:n.-165G>A
ENST00000509016.5:n.1G>A
ENST00000513428.5:n.1G>A
ENST00000513523.1:n.4G>A
NM_001154.3:c.-165G>A NP_001145.1:n.-165G>A
XM_017008141.2:c.-165G>A XP_016863630.1:n.-165G>A
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