Canonical Allele Identifier: CA790668077
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1318767145
gnomAD v3: 4-168165582-T-C
gnomAD v4: 4-168165582-T-C
MyVariant Identifiers: chr4:g.169086733T>C (hg19) chr4:g.168165582T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165582T>C , CM000666.2:g.168165582T>C GRCh38
NC_000004.11:g.169086733T>C , CM000666.1:g.169086733T>C GRCh37
NC_000004.10:g.169323308T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+256T>C MANE Select ENSP00000352248.3:n.480+256T>C
ENST00000359299.7:c.480+256T>C ENSP00000352248.3:n.480+256T>C
ENST00000503003.1:n.86+256T>C
ENST00000507278.5:n.143+256T>C
ENST00000617524.1:c.477+256T>C ENSP00000483710.1:n.477+256T>C
NM_007193.4:c.480+256T>C NP_009124.2:n.480+256T>C
XM_011531571.1:c.540+256T>C XP_011529873.1:n.540+256T>C
XM_011531571.2:c.540+256T>C XP_011529873.1:n.540+256T>C
NM_007193.5:c.480+256T>C MANE Select NP_009124.2:n.480+256T>C
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