Canonical Allele Identifier: CA2491383607
Gene:

Linked Data

dbSNP Id: rs1664551652

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458193A>T , CM000664.2:g.16458193A>T GRCh38
NC_000002.11:g.16639461A>T , CM000664.1:g.16639461A>T GRCh37
NC_000002.10:g.16502942A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3099T>A