Canonical Allele Identifier: CA786357930
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1275248493
gnomAD v3: 4-121697015-C-A
gnomAD v4: 4-121697015-C-A
MyVariant Identifiers: chr4:g.122618170C>A (hg19) chr4:g.121697015C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121697015C>A , CM000666.2:g.121697015C>A GRCh38
NC_000004.11:g.122618170C>A , CM000666.1:g.122618170C>A GRCh37
NC_000004.10:g.122837620C>A NCBI36
NG_032042.1:g.4978G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-188G>T ENSP00000296511.5:n.-188G>T
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