Canonical Allele Identifier: CA786357899
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1448037040
gnomAD v3: 4-121696989-C-G
gnomAD v4: 4-121696989-C-G
MyVariant Identifiers: chr4:g.122618144C>G (hg19) chr4:g.121696989C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696989C>G , CM000666.2:g.121696989C>G GRCh38
NC_000004.11:g.122618144C>G , CM000666.1:g.122618144C>G GRCh37
NC_000004.10:g.122837594C>G NCBI36
NG_032042.1:g.5004G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.9:c.-162G>C ENSP00000296511.5:n.-162G>C
ENST00000509016.5:n.4G>C
ENST00000513428.5:n.4G>C
ENST00000513523.1:n.7G>C
NM_001154.3:c.-162G>C NP_001145.1:n.-162G>C
XM_017008141.2:c.-162G>C XP_016863630.1:n.-162G>C
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