Canonical Allele Identifier: CA240569168
Gene:

Linked Data

dbSNP Id: rs897630236

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069248T>G , CM000674.2:g.80069248T>G GRCh38
NC_000012.11:g.80463028T>G , CM000674.1:g.80463028T>G GRCh37
NC_000012.10:g.78987159T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8066T>G
XR_945141.1:n.1758+8066T>G