Canonical Allele Identifier: CA1458424540
Gene:

Linked Data

dbSNP Id: rs1717635587

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072455G>A , CM000666.2:g.54072455G>A GRCh38
NC_000004.11:g.54938622G>A , CM000666.1:g.54938622G>A GRCh37
NC_000004.10:g.54633379G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202470G>A ENSP00000423325.1:n.1018-202470G>A