Canonical Allele Identifier: CA2223789374
Gene:

Linked Data

dbSNP Id: rs1964423739

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655474G>A , CM000678.2:g.55655474G>A GRCh38
NC_000016.9:g.55689386G>A , CM000678.1:g.55689386G>A GRCh37
NC_000016.8:g.54246887G>A NCBI36
NG_016969.1:g.4845G>A

Transcript Alleles

HGVS Amino-acid change
XR_933603.1:n.54+125C>T