Canonical Allele Identifier: CA2491383700
Gene:

Linked Data

dbSNP Id: rs1664554468

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458400T>C , CM000664.2:g.16458400T>C GRCh38
NC_000002.11:g.16639668T>C , CM000664.1:g.16639668T>C GRCh37
NC_000002.10:g.16503149T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3306A>G