Canonical Allele Identifier: CA10815368
Gene: ANXA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150989393A>G , CM000663.2:g.150989393A>G GRCh38
NC_000001.10:g.150961869A>G , CM000663.1:g.150961869A>G GRCh37
NC_000001.9:g.149228493A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368947.9:c.852+1052A>G MANE Select ENSP00000357943.4:n.852+1052A>G
ENST00000368947.8:c.852+1052A>G ENSP00000357943.4:n.852+1052A>G
NM_003568.2:c.852+1052A>G NP_003559.2:n.852+1052A>G
XM_005245539.3:c.852+1052A>G XP_005245596.1:n.852+1052A>G
XM_011510058.1:c.852+1052A>G XP_011508360.1:n.852+1052A>G
XM_011510058.3:c.852+1052A>G XP_011508360.1:n.852+1052A>G
NM_003568.3:c.852+1052A>G MANE Select NP_003559.2:n.852+1052A>G