Canonical Allele Identifier: CA185200403
Gene:

Linked Data

dbSNP Id: rs370296820

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395862C>T , CM000670.2:g.122395862C>T GRCh38
NC_000008.10:g.123408101C>T , CM000670.1:g.123408101C>T GRCh37
NC_000008.9:g.123477282C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3310G>A
XR_928599.3:n.152+3310G>A