Canonical Allele Identifier: CA30892285
Gene:

Linked Data

dbSNP Id: rs2070803
MyVariant Identifiers: chr1:g.155185239G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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