Canonical Allele Identifier: CA1206219169

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169736983C= , CM000663.2:g.169736983C= GRCh38
NC_000001.10:g.169706124C= , CM000663.1:g.169706124C= GRCh37
NC_000001.9:g.167972748C= NCBI36
NG_012124.1:g.2097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.852-46828C= (FIRRM)
ENST00000609271.1:c.-201-2860G= (SELE) ENSP00000476784.1:n.-201-2860G=