Canonical Allele Identifier: CA2481181567
Gene:

Linked Data

dbSNP Id: rs2070803

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155185239G>T , CM000663.2:g.155185239G>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000473363.3:c.48+1986C>A ENSP00000477381.3:n.48+1986C>A
ENST00000473363.2:c.48+1986C>A