Canonical Allele Identifier: CA109807959
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1018896419
gnomAD v3: 4-168165599-A-G
gnomAD v4: 4-168165599-A-G
MyVariant Identifiers: chr4:g.169086750A>G (hg19) chr4:g.168165599A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165599A>G , CM000666.2:g.168165599A>G GRCh38
NC_000004.11:g.169086750A>G , CM000666.1:g.169086750A>G GRCh37
NC_000004.10:g.169323325A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+273A>G MANE Select ENSP00000352248.3:n.480+273A>G
ENST00000359299.7:c.480+273A>G ENSP00000352248.3:n.480+273A>G
ENST00000503003.1:n.86+273A>G
ENST00000507278.5:n.143+273A>G
ENST00000617524.1:c.477+273A>G ENSP00000483710.1:n.477+273A>G
NM_007193.4:c.480+273A>G NP_009124.2:n.480+273A>G
XM_011531571.1:c.540+273A>G XP_011529873.1:n.540+273A>G
XM_011531571.2:c.540+273A>G XP_011529873.1:n.540+273A>G
NM_007193.5:c.480+273A>G MANE Select NP_009124.2:n.480+273A>G
Search 100 bp 5'
Search 100 bp 3'