Canonical Allele Identifier: CA1206219168

Gene: FIRRM SELE

Linked Data

• dbSNP Id: rs1649068413

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169736981C>A , CM000663.2:g.169736981C>A	GRCh38
NC_000001.10:g.169706122C>A , CM000663.1:g.169706122C>A	GRCh37
NC_000001.9:g.167972746C>A	NCBI36
NG_012124.1:g.2099G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498289.5:n.852-46830C>A (FIRRM)
ENST00000609271.1:c.-201-2858G>T (SELE)	ENSP00000476784.1:n.-201-2858G>T