Canonical Allele Identifier: CA2022606233
Gene:

Linked Data

dbSNP Id: rs1598004857

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.24617874T>C , CM000674.2:g.24617874T>C GRCh38
NC_000012.11:g.24770808T>C , CM000674.1:g.24770808T>C GRCh37
NC_000012.10:g.24662075T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749046.1:n.425-64A>G