Canonical Allele Identifier: CA32487521
Gene: FIRRM HGNC NCBI
SELE HGNC NCBI

Linked Data

dbSNP Id: rs1044205638
MyVariant Identifiers: chr1:g.169706007T>A (hg19) chr1:g.169736866T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169736866T>A , CM000663.2:g.169736866T>A GRCh38
NC_000001.10:g.169706007T>A , CM000663.1:g.169706007T>A GRCh37
NC_000001.9:g.167972631T>A NCBI36
NG_012124.1:g.2214A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000498289.5:n.852-46945T>A (FIRRM)
ENST00000609271.1:c.-201-2743A>T (SELE) ENSP00000476784.1:n.-201-2743A>T
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