Canonical Allele Identifier: CA32487583

Gene: FIRRM SELE

Linked Data

• dbSNP Id: rs1044501584
• gnomAD v3: 1-169736974-G-A
• gnomAD v4: 1-169736974-G-A
• MyVariant Identifiers: chr1:g.169706115G>A (hg19) ; chr1:g.169736974G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169736974G>A , CM000663.2:g.169736974G>A	GRCh38
NC_000001.10:g.169706115G>A , CM000663.1:g.169706115G>A	GRCh37
NC_000001.9:g.167972739G>A	NCBI36
NG_012124.1:g.2106C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498289.5:n.852-46837G>A (FIRRM)
ENST00000609271.1:c.-201-2851C>T (SELE)	ENSP00000476784.1:n.-201-2851C>T