Canonical Allele Identifier: CA2491383698

Gene:

Linked Data

• dbSNP Id: rs1664554435

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.16458393A>T , CM000664.2:g.16458393A>T	GRCh38
NC_000002.11:g.16639661A>T , CM000664.1:g.16639661A>T	GRCh37
NC_000002.10:g.16503142A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939752.1:n.396-3299T>A