Canonical Allele Identifier: CA18888247
Gene:

Linked Data

dbSNP Id: rs4654903

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19874497A>C , CM000663.2:g.19874497A>C GRCh38
NC_000001.10:g.20200990A>C , CM000663.1:g.20200990A>C GRCh37
NC_000001.9:g.20073577A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947027.1:n.266-8745T>G
XR_947028.1:n.266-8745T>G
XR_947027.2:n.167-8745T>G
XR_947028.2:n.167-8745T>G