Canonical Allele Identifier: CA554176764
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1448492905
gnomAD v2: 4-122618203-C-T
gnomAD v3: 4-121697048-C-T
gnomAD v4: 4-121697048-C-T
MyVariant Identifiers: chr4:g.122618203C>T (hg19) chr4:g.121697048C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121697048C>T , CM000666.2:g.121697048C>T GRCh38
NC_000004.11:g.122618203C>T , CM000666.1:g.122618203C>T GRCh37
NC_000004.10:g.122837653C>T NCBI36
NG_032042.1:g.4945G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-221G>A ENSP00000296511.5:n.-221G>A
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