Canonical Allele Identifier: CA2725530872
Gene:

Linked Data

dbSNP Id: rs2136673806

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276580A>C , CM000674.2:g.6276580A>C GRCh38
NC_000012.11:g.6385746A>C , CM000674.1:g.6385746A>C GRCh37
NC_000012.10:g.6256007A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748976.1:n.157+16519T>G
XR_001748977.1:n.157+16519T>G
XR_001748978.1:n.157+16519T>G
XR_001748979.1:n.157+16519T>G
XR_001748980.1:n.157+16519T>G