Canonical Allele Identifier: CA2491383651
Gene:

Linked Data

dbSNP Id: rs1664553024

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458280A>G , CM000664.2:g.16458280A>G GRCh38
NC_000002.11:g.16639548A>G , CM000664.1:g.16639548A>G GRCh37
NC_000002.10:g.16503029A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3186T>C