Canonical Allele Identifier: CA12798039
Gene:

Linked Data

dbSNP Id: rs1902432

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012566A>G , CM000670.2:g.127012566A>G GRCh38
NC_000008.10:g.128024811A>G , CM000670.1:g.128024811A>G GRCh37
NC_000008.9:g.128093993A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1364+5948A>G