Canonical Allele Identifier: CA1188354877

Linked Data

dbSNP Id: rs1653730452

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064522A>G , CM000663.2:g.110064522A>G GRCh38
NC_000001.10:g.110607144A>G , CM000663.1:g.110607144A>G GRCh37
NC_000001.9:g.110408667A>G NCBI36
NG_012039.1:g.11179T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.594+65T>C (ALX3) MANE Select ENSP00000497310.1:n.594+65T>C
ENST00000649954.1:c.165+65T>C (ALX3) ENSP00000497035.1:n.165+65T>C
ENST00000369792.4:c.594+65T>C (ALX3) ENSP00000358807.3:n.594+65T>C
ENST00000473429.5:n.4214-7933A>G (STRIP1)
NM_006492.2:c.594+65T>C (ALX3) NP_006483.2:n.594+65T>C
NM_006492.3:c.594+65T>C (ALX3) MANE Select NP_006483.2:n.594+65T>C