Canonical Allele Identifier: CA2492005207
Gene:

Linked Data

dbSNP Id: rs1673969734

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844036G>A , CM000664.2:g.17844036G>A GRCh38
NC_000002.11:g.18025303G>A , CM000664.1:g.18025303G>A GRCh37
NC_000002.10:g.17888784G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3658C>T