Canonical Allele Identifier: CA554176770
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1018424424
gnomAD v2: 4-122618216-C-T
gnomAD v3: 4-121697061-C-T
gnomAD v4: 4-121697061-C-T
MyVariant Identifiers: chr4:g.122618216C>T (hg19) chr4:g.121697061C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121697061C>T , CM000666.2:g.121697061C>T GRCh38
NC_000004.11:g.122618216C>T , CM000666.1:g.122618216C>T GRCh37
NC_000004.10:g.122837666C>T NCBI36
NG_032042.1:g.4932G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-234G>A ENSP00000296511.5:n.-234G>A
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