Canonical Allele Identifier: CA1775343188
Gene:

Linked Data

dbSNP Id: rs1802343277

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808410A>T , CM000670.2:g.33808410A>T GRCh38
NC_000008.10:g.33665928A>T , CM000670.1:g.33665928A>T GRCh37
NC_000008.9:g.33785470A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11974A>T
XR_002956701.1:n.240+11974A>T