Canonical Allele Identifier: CA104731822
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs558420537
gnomAD v3: 4-121696993-G-C
gnomAD v4: 4-121696993-G-C
MyVariant Identifiers: chr4:g.122618148G>C (hg19) chr4:g.121696993G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696993G>C , CM000666.2:g.121696993G>C GRCh38
NC_000004.11:g.122618148G>C , CM000666.1:g.122618148G>C GRCh37
NC_000004.10:g.122837598G>C NCBI36
NG_032042.1:g.5000C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-166C>G ENSP00000296511.5:n.-166C>G
ENST00000513523.1:n.3C>G
XM_017008141.2:c.-166C>G XP_016863630.1:n.-166C>G
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