Canonical Allele Identifier: CA555999449
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1306712862
gnomAD v2: 4-169086565-G-A
gnomAD v3: 4-168165414-G-A
gnomAD v4: 4-168165414-G-A
MyVariant Identifiers: chr4:g.169086565G>A (hg19) chr4:g.168165414G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165414G>A , CM000666.2:g.168165414G>A GRCh38
NC_000004.11:g.169086565G>A , CM000666.1:g.169086565G>A GRCh37
NC_000004.10:g.169323140G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+88G>A MANE Select ENSP00000352248.3:n.480+88G>A
ENST00000359299.7:c.480+88G>A ENSP00000352248.3:n.480+88G>A
ENST00000503003.1:n.86+88G>A
ENST00000507278.5:n.143+88G>A
ENST00000617524.1:c.477+88G>A ENSP00000483710.1:n.477+88G>A
NM_007193.4:c.480+88G>A NP_009124.2:n.480+88G>A
XM_011531571.1:c.540+88G>A XP_011529873.1:n.540+88G>A
XM_011531571.2:c.540+88G>A XP_011529873.1:n.540+88G>A
NM_007193.5:c.480+88G>A MANE Select NP_009124.2:n.480+88G>A
Search 100 bp 5'
Search 100 bp 3'