Canonical Allele Identifier: CA554176766
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1300867282
gnomAD v2: 4-122618210-CCCAACCGCAGGCCGGCCGCG-C
gnomAD v3: 4-121697055-CCCAACCGCAGGCCGGCCGCG-C
gnomAD v4: 4-121697055-CCCAACCGCAGGCCGGCCGCG-C
MyVariant Identifiers: chr4:g.122618211_122618230del (hg19) chr4:g.121697056_121697075del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121697059_121697078del , CM000666.2:g.121697059_121697078del GRCh38
NC_000004.11:g.122618214_122618233del , CM000666.1:g.122618214_122618233del GRCh37
NC_000004.10:g.122837664_122837683del NCBI36
NG_032042.1:g.4918_4937del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-248_-229del ENSP00000296511.5:n.-248_-229del
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