Canonical Allele Identifier: CA554176754

Gene: ANXA5

Linked Data

• dbSNP Id: rs1237710594
• gnomAD v2: 4-122618157-A-C
• gnomAD v3: 4-121697002-A-C
• gnomAD v4: 4-121697002-A-C
• MyVariant Identifiers: chr4:g.122618157A>C (hg19) ; chr4:g.121697002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121697002A>C , CM000666.2:g.121697002A>C	GRCh38
NC_000004.11:g.122618157A>C , CM000666.1:g.122618157A>C	GRCh37
NC_000004.10:g.122837607A>C	NCBI36
NG_032042.1:g.4991T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.9:c.-175T>G	ENSP00000296511.5:n.-175T>G