Canonical Allele Identifier: CA1816081218
Gene:

Linked Data

dbSNP Id: rs907568871

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395855A>T , CM000670.2:g.122395855A>T GRCh38
NC_000008.10:g.123408094A>T , CM000670.1:g.123408094A>T GRCh37
NC_000008.9:g.123477275A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3317T>A
XR_928599.3:n.152+3317T>A