Canonical Allele Identifier: CA790668008
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1388148366
MyVariant Identifiers: chr4:g.169086627G>C (hg19) chr4:g.168165476G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165476G>C , CM000666.2:g.168165476G>C GRCh38
NC_000004.11:g.169086627G>C , CM000666.1:g.169086627G>C GRCh37
NC_000004.10:g.169323202G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+150G>C MANE Select ENSP00000352248.3:n.480+150G>C
ENST00000359299.7:c.480+150G>C ENSP00000352248.3:n.480+150G>C
ENST00000503003.1:n.86+150G>C
ENST00000507278.5:n.143+150G>C
ENST00000617524.1:c.477+150G>C ENSP00000483710.1:n.477+150G>C
NM_007193.4:c.480+150G>C NP_009124.2:n.480+150G>C
XM_011531571.1:c.540+150G>C XP_011529873.1:n.540+150G>C
XM_011531571.2:c.540+150G>C XP_011529873.1:n.540+150G>C
NM_007193.5:c.480+150G>C MANE Select NP_009124.2:n.480+150G>C
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